| Trait Information | |
| Identifier | MONDO_0002562 |
| Description | A broad group of disorders that affect the myelin sheaths that cover the neurons. Myelin sheathes cover neuronal axons in the central and peripheral nervous system and function to increase traveling impulse speeds. Disruption of this sheath impairs neuronal transmission and can result in disorders such as multiple sclerosis and Guillain-Barre syndrome, among others. [NCIT: P378] | Trait category |
Other trait
|
| Synonym | demyelinating disorder |
| Child trait(s) | multiple sclerosis |
| Polygenic Score ID & Name | PGS Publication ID (PGP) | Reported Trait | Mapped Trait(s) (Ontology) | Number of Variants |
Ancestry distribution GWAS Dev Eval |
Scoring File (FTP Link) |
|---|---|---|---|---|---|---|
| PGS000809 (PRS127_MS) |
PGP000194 | Barnes CLK et al. Eur J Hum Genet (2021) |
Multiple sclerosis | multiple sclerosis | 127 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS000809/ScoringFiles/PGS000809.txt.gz |
| PGS001270 (GBE_HC151) |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Multiple sclerosis | multiple sclerosis | 41 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS001270/ScoringFiles/PGS001270.txt.gz |
| PGS001271 (GBE_HC810) |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Multiple sclerosis (time-to-event) | multiple sclerosis | 36 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS001271/ScoringFiles/PGS001271.txt.gz |
| PGS001831 (portability-PLR_335) |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Multiple sclerosis | multiple sclerosis | 491 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS001831/ScoringFiles/PGS001831.txt.gz |
| PGS002038 (portability-ldpred2_335) |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Multiple sclerosis | multiple sclerosis | 129,077 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS002038/ScoringFiles/PGS002038.txt.gz |
| PGS002726 (PGS_MS_Brain) |
PGP000334 | Shams H et al. Brain (2022) |
Multiple sclerosis | multiple sclerosis | 476,399 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS002726/ScoringFiles/PGS002726.txt.gz |
| PGS004699 (Non-HLA-GRS) |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Multiple sclerosis | multiple sclerosis | 307 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS004699/ScoringFiles/PGS004699.txt.gz |
| PGS004700 (HLA-GRS) |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Multiple sclerosis | multiple sclerosis | 12 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS004700/ScoringFiles/PGS004700.txt.gz |
|
PGS Performance Metric ID (PPM) |
Evaluated Score |
PGS Sample Set ID (PSS) |
Performance Source | Trait |
PGS Effect Sizes (per SD change) |
Classification Metrics | Other Metrics | Covariates Included in the Model |
PGS Performance: Other Relevant Information |
|---|---|---|---|---|---|---|---|---|---|
| PPM002137 | PGS000809 (PRS127_MS) |
PSS001050| European Ancestry| 725 individuals |
PGP000194 | Barnes CLK et al. Eur J Hum Genet (2021) |
Reported Trait: Multiple sclerosis | β: 0.6 | AUROC: 0.705 (0.029) | R²: 0.07 | Age, sex, PCs(1-2) | — |
| PPM002138 | PGS000809 (PRS127_MS) |
PSS001051| European Ancestry| 656 individuals |
PGP000194 | Barnes CLK et al. Eur J Hum Genet (2021) |
Reported Trait: Multiple sclerosis | β: 0.59 | AUROC: 0.762 (0.055) | R²: 0.075 | Age, sex, PCs(1-2) | — |
| PPM002139 | PGS000809 (PRS127_MS) |
PSS001049| European Ancestry| 8,370 individuals |
PGP000194 | Barnes CLK et al. Eur J Hum Genet (2021) |
Reported Trait: Multiple Sclerosis | β: 0.63 | AUROC: 0.765 (0.042) | R²: 0.069 | Age, sex, PCs(1-2) | — |
| PPM008850 | PGS001270 (GBE_HC151) |
PSS004273| African Ancestry| 6,497 individuals |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.78603 [0.68344, 0.88862] | R²: 0.07124 Incremental AUROC (full-covars): -0.04449 PGS R2 (no covariates): 0.02639 PGS AUROC (no covariates): 0.35945 [0.2174, 0.5015] |
age, sex, UKB array type, Genotype PCs | Full Model & PGS R2 is estimated using Nagelkerke's method |
| PPM008851 | PGS001270 (GBE_HC151) |
PSS004274| European Ancestry| 24,905 individuals |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.65766 [0.60651, 0.7088] | R²: 0.02306 Incremental AUROC (full-covars): 0.0559 PGS R2 (no covariates): 0.01225 PGS AUROC (no covariates): 0.61627 [0.56233, 0.67022] |
age, sex, UKB array type, Genotype PCs | Full Model & PGS R2 is estimated using Nagelkerke's method |
| PPM008852 | PGS001270 (GBE_HC151) |
PSS004275| South Asian Ancestry| 7,831 individuals |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.9739 [0.9358, 1.0] | R²: 0.3229 Incremental AUROC (full-covars): 0.01955 PGS R2 (no covariates): 0.02901 PGS AUROC (no covariates): 0.64875 [0.24603, 1.0] |
age, sex, UKB array type, Genotype PCs | Full Model & PGS R2 is estimated using Nagelkerke's method |
| PPM008853 | PGS001270 (GBE_HC151) |
PSS004276| European Ancestry| 67,425 individuals |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.69658 [0.66502, 0.72814] | R²: 0.04105 Incremental AUROC (full-covars): 0.08355 PGS R2 (no covariates): 0.02904 PGS AUROC (no covariates): 0.65856 [0.62428, 0.69284] |
age, sex, UKB array type, Genotype PCs | Full Model & PGS R2 is estimated using Nagelkerke's method |
| PPM008854 | PGS001271 (GBE_HC810) |
PSS004637| African Ancestry| 6,497 individuals |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Reported Trait: TTE multiple sclerosis | — | AUROC: 0.8033 [0.6935, 0.91311] | PGS R2 (no covariates): 0.01095 R²: 0.10788 Incremental AUROC (full-covars): -0.03509 PGS AUROC (no covariates): 0.39974 [0.23738, 0.56211] |
age, sex, UKB array type, Genotype PCs | Full Model & PGS R2 is estimated using Nagelkerke's method |
| PPM008855 | PGS001271 (GBE_HC810) |
PSS004639| European Ancestry| 24,905 individuals |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Reported Trait: TTE multiple sclerosis | — | AUROC: 0.65561 [0.60622, 0.705] | R²: 0.02347 Incremental AUROC (full-covars): 0.05454 PGS R2 (no covariates): 0.01258 PGS AUROC (no covariates): 0.61601 [0.56326, 0.66875] |
age, sex, UKB array type, Genotype PCs | Full Model & PGS R2 is estimated using Nagelkerke's method |
| PPM008856 | PGS001271 (GBE_HC810) |
PSS004640| South Asian Ancestry| 7,831 individuals |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Reported Trait: TTE multiple sclerosis | — | AUROC: 0.97595 [0.94159, 1.0] | R²: 0.33555 Incremental AUROC (full-covars): 0.01648 PGS R2 (no covariates): 0.01091 PGS AUROC (no covariates): 0.55629 [0.19512, 0.91745] |
age, sex, UKB array type, Genotype PCs | Full Model & PGS R2 is estimated using Nagelkerke's method |
| PPM008857 | PGS001271 (GBE_HC810) |
PSS004641| European Ancestry| 67,425 individuals |
PGP000244 | Tanigawa Y et al. PLoS Genet (2022) |
Reported Trait: TTE multiple sclerosis | — | AUROC: 0.6895 [0.65926, 0.71974] | R²: 0.03906 Incremental AUROC (full-covars): 0.07145 PGS R2 (no covariates): 0.02562 PGS AUROC (no covariates): 0.64688 [0.61364, 0.68013] |
age, sex, UKB array type, Genotype PCs | Full Model & PGS R2 is estimated using Nagelkerke's method |
| PPM009541 | PGS001831 (portability-PLR_335) |
PSS009301| European Ancestry| 19,299 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0367 [0.0226, 0.0508] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM009542 | PGS001831 (portability-PLR_335) |
PSS009075| European Ancestry| 4,011 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0122 [-0.0188, 0.0432] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM009543 | PGS001831 (portability-PLR_335) |
PSS008629| European Ancestry| 6,463 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0578 [0.0334, 0.0821] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM009544 | PGS001831 (portability-PLR_335) |
PSS008403| Greater Middle Eastern Ancestry| 1,164 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0242 [-0.0338, 0.082] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM009545 | PGS001831 (portability-PLR_335) |
PSS008183| South Asian Ancestry| 6,094 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0064 [-0.0188, 0.0315] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM009546 | PGS001831 (portability-PLR_335) |
PSS007749| African Ancestry| 2,390 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0032 [-0.037, 0.0435] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM009547 | PGS001831 (portability-PLR_335) |
PSS008853| African Ancestry| 3,790 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): -0.0104 [-0.0423, 0.0216] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM011172 | PGS002038 (portability-ldpred2_335) |
PSS009075| European Ancestry| 4,011 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0083 [-0.0228, 0.0393] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM011173 | PGS002038 (portability-ldpred2_335) |
PSS008629| European Ancestry| 6,463 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0447 [0.0203, 0.069] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM011174 | PGS002038 (portability-ldpred2_335) |
PSS008403| Greater Middle Eastern Ancestry| 1,164 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0296 [-0.0284, 0.0874] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM011175 | PGS002038 (portability-ldpred2_335) |
PSS008183| South Asian Ancestry| 6,094 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0149 [-0.0103, 0.04] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM011176 | PGS002038 (portability-ldpred2_335) |
PSS007749| African Ancestry| 2,390 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.006 [-0.0343, 0.0463] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM011177 | PGS002038 (portability-ldpred2_335) |
PSS008853| African Ancestry| 3,790 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): -0.0243 [-0.0561, 0.0077] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM011171 | PGS002038 (portability-ldpred2_335) |
PSS009301| European Ancestry| 19,299 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Multiple sclerosis | — | — | Partial Correlation (partial-r): 0.0396 [0.0255, 0.0536] | sex, age, birth date, deprivation index, 16 PCs | — |
| PPM014749 | PGS002726 (PGS_MS_Brain) |
PSS009883| European Ancestry| 253,419 individuals |
PGP000334 | Shams H et al. Brain (2022) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.73 [0.72, 0.74] | Odds ratio (OR, top 10% vs median): 5.3 [4.7, 6.0] | — | — |
| PPM014750 | PGS002726 (PGS_MS_Brain) |
PSS009882| European Ancestry| 938 individuals |
PGP000334 | Shams H et al. Brain (2022) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.8 [0.76, 0.82] | Odds ratio (OR, top 10% vs median): 15.0 [10.4, 24.0] | — | — |
| PPM020918 | PGS004699 (Non-HLA-GRS) |
PSS011453| Multi-ancestry (including European)| 483,480 individuals |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.752 [0.75, 0.755] | — | Age at recruitment, sex, Townsend Deprivation Index, 4 PCs | NOTE: Performance is based on an unweighted sum of Non-HLA-GRS and HLA-GRS |
| PPM020919 | PGS004699 (Non-HLA-GRS) |
PSS011452| Multi-ancestry (including European)| 116,767 individuals |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.744 | — | Index age, reported sex, 4 PCs | NOTE: Performance is based on an unweighted sum of Non-HLA-GRS and HLA-GRS |
| PPM020920 | PGS004699 (Non-HLA-GRS) |
PSS011451| Ancestry Not Reported| 372,416 individuals |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.764 | — | Age at DNA sample collection, sex, 4 PCs | NOTE: Performance is based on an unweighted sum of Non-HLA-GRS and HLA-GRS |
| PPM020921 | PGS004699 (Non-HLA-GRS) |
PSS011454| Multi-ancestry (including European)| 545 individuals |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Reported Trait: Multiple sclerosis in individuals with undifferentiated optic neuritis | HR: 1.29 [1.07, 1.55] | — | — | Age, sex | NOTE: Performance is based on an unweighted sum of Non-HLA-GRS and HLA-GRS |
| PPM020922 | PGS004700 (HLA-GRS) |
PSS011453| Multi-ancestry (including European)| 483,480 individuals |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.752 [0.75, 0.755] | — | Age at recruitment, sex, Townsend Deprivation Index, 4 PCs | NOTE: Performance is based on an unweighted sum of Non-HLA-GRS and HLA-GRS |
| PPM020923 | PGS004700 (HLA-GRS) |
PSS011452| Multi-ancestry (including European)| 116,767 individuals |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.744 | — | Index age, reported sex, 4 PCs | NOTE: Performance is based on an unweighted sum of Non-HLA-GRS and HLA-GRS |
| PPM020924 | PGS004700 (HLA-GRS) |
PSS011451| Ancestry Not Reported| 372,416 individuals |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Reported Trait: Multiple sclerosis | — | AUROC: 0.764 | — | Age at DNA sample collection, sex, 4 PCs | NOTE: Performance is based on an unweighted sum of Non-HLA-GRS and HLA-GRS |
| PPM020925 | PGS004700 (HLA-GRS) |
PSS011454| Multi-ancestry (including European)| 545 individuals |
PGP000603 | Loginovic P et al. Nat Commun (2024) |
Reported Trait: Multiple sclerosis in individuals with undifferentiated optic neuritis | HR: 1.29 [1.07, 1.55] | — | — | Age, sex | NOTE: Performance is based on an unweighted sum of Non-HLA-GRS and HLA-GRS |
|
PGS Sample Set ID (PSS) |
Phenotype Definitions and Methods | Participant Follow-up Time | Sample Numbers | Age of Study Participants | Sample Ancestry | Additional Ancestry Description | Cohort(s) | Additional Sample/Cohort Information |
|---|---|---|---|---|---|---|---|---|
| PSS007749 | — | — | 2,390 individuals | — | African American or Afro-Caribbean | Carribean | UKB | — |
| PSS008403 | — | — | 1,164 individuals | — | Greater Middle Eastern (Middle Eastern, North African or Persian) | Iran (Middle East) | UKB | — |
| PSS009301 | — | — | 19,299 individuals | — | European | UK (+ Ireland) | UKB | — |
| PSS009075 | — | — | 4,011 individuals | — | European | Poland (NE Europe) | UKB | — |
| PSS008183 | — | — | 6,094 individuals | — | South Asian | India (South Asia) | UKB | — |
| PSS011451 | — | — | [
|
— | Not reported | — | FinnGen | — |
| PSS011452 | — | — | [
|
— | European | — | MyCode | — |
| PSS011452 | — | — | [
|
— | Not reported | — | MyCode | — |
| PSS011453 | — | — | [
|
— | European | — | UKB | — |
| PSS011453 | — | — | [
|
— | Not reported | — | UKB | — |
| PSS011454 | — | — | 462 individuals | — | European | — | UKB | — |
| PSS011454 | — | — | 83 individuals | — | Not reported | — | UKB | — |
| PSS009882 | — | — | [
|
— | European | — | KP | — |
| PSS009883 | — | — | [
|
— | European | — | UKB | — |
| PSS008853 | — | — | 3,790 individuals | — | African unspecified | Nigeria (West Africa) | UKB | — |
| PSS001049 | Cases are individuals with multiple sclerosis. | — | [
|
— | European | Mainland Scotland | GS:SFHS | — |
| PSS001050 | Cases are individuals with multiple sclerosis. | — | [
|
— | European | Orkney | ORCADES | — |
| PSS001051 | Cases are individuals with multiple sclerosis. | — | [
|
— | European | Shetlands | VIKING | — |
| PSS004637 | — | — | [
|
— | African unspecified | — | UKB | — |
| PSS004639 | — | — | [
|
— | European | non-white British ancestry | UKB | — |
| PSS004640 | — | — | [
|
— | South Asian | — | UKB | — |
| PSS004641 | — | — | [
|
— | European | white British ancestry | UKB | Testing cohort (heldout set) |
| PSS008629 | — | — | 6,463 individuals | — | European | Italy (South Europe) | UKB | — |
| PSS004273 | — | — | [
|
— | African unspecified | — | UKB | — |
| PSS004274 | — | — | [
|
— | European | non-white British ancestry | UKB | — |
| PSS004275 | — | — | [
|
— | South Asian | — | UKB | — |
| PSS004276 | — | — | [
|
— | European | white British ancestry | UKB | Testing cohort (heldout set) |