rs9523762
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9523762(A;A) |
| Make rs9523762(A;G) |
| Make rs9523762(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 92679633 |
| Gene | GPC5, LOC105370315 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9523762 |
| dbSNP (classic) | rs9523762 |
| ClinGen | rs9523762 |
| ebi | rs9523762 |
| HLI | rs9523762 |
| Exac | rs9523762 |
| Gnomad | rs9523762 |
| Varsome | rs9523762 |
| LitVar | rs9523762 |
| Map | rs9523762 |
| PheGenI | rs9523762 |
| Biobank | rs9523762 |
| 1000 genomes | rs9523762 |
| hgdp | rs9523762 |
| ensembl | rs9523762 |
| geneview | rs9523762 |
| scholar | rs9523762 |
| rs9523762 | |
| pharmgkb | rs9523762 |
| gwascentral | rs9523762 |
| openSNP | rs9523762 |
| 23andMe | rs9523762 |
| SNPshot | rs9523762 |
| SNPdbe | rs9523762 |
| MSV3d | rs9523762 |
| GWAS Ctlg | rs9523762 |
| GMAF | 0.4376 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19010793 ]
|
| Trait | Multiple sclerosis |
| Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
| Risk Allele | |
| P-val | 0.000001 |
| Odds Ratio | 1.36 [NR] |
[PMID 20182566] The genetic aspects of multiple sclerosis.
[PMID 20405052] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
[PMID 20944657] Replication of top markers of a genome-wide association study in multiple sclerosis in Spain.
