rs9468925
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9468925(A;A) |
Make rs9468925(A;G) |
Make rs9468925(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31291060 |
Gene | WASF5P |
is a | snp |
is | mentioned by |
dbSNP | rs9468925 |
dbSNP (classic) | rs9468925 |
ClinGen | rs9468925 |
ebi | rs9468925 |
HLI | rs9468925 |
Exac | rs9468925 |
Gnomad | rs9468925 |
Varsome | rs9468925 |
LitVar | rs9468925 |
Map | rs9468925 |
PheGenI | rs9468925 |
Biobank | rs9468925 |
1000 genomes | rs9468925 |
hgdp | rs9468925 |
ensembl | rs9468925 |
geneview | rs9468925 |
scholar | rs9468925 |
rs9468925 | |
pharmgkb | rs9468925 |
gwascentral | rs9468925 |
openSNP | rs9468925 |
23andMe | rs9468925 |
SNPshot | rs9468925 |
SNPdbe | rs9468925 |
MSV3d | rs9468925 |
GWAS Ctlg | rs9468925 |
GMAF | 0.4518 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20526339] |
Trait | Vitiligo |
Title | Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC |
Risk Allele | |
P-val | 2E-33 |
Odds Ratio | 1.35 [1.28-1.41] |
[PMID 21951294] A single nucleotide polymorphism rs9468925 of MHC region is associated with clinical features of generalized vitiligo in Chinese Han population
[PMID 20017995] A principal-components-based clustering method to identify multiple variants associated with rheumatoid arthritis and arthritis-related autoantibodies.