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rs9468925

From SNPedia

Orientationplus
Stabilizedplus
Make rs9468925(A;A)
Make rs9468925(A;G)
Make rs9468925(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31291060
GeneWASF5P
is asnp
is mentioned by
dbSNPrs9468925
ebirs9468925
HLIrs9468925
Exacrs9468925
Varsomers9468925
Maprs9468925
PheGenIrs9468925
hapmaprs9468925
1000 genomesrs9468925
hgdprs9468925
ensemblrs9468925
gopubmedrs9468925
geneviewrs9468925
scholarrs9468925
googlers9468925
pharmgkbrs9468925
gwascentralrs9468925
openSNPrs9468925
23andMers9468925
23andMe allrs9468925
SNP Nexus

SNPshotrs9468925
SNPdbers9468925
MSV3drs9468925
GWAS Ctlgrs9468925
GMAF0.4518
Max Magnitude
? (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]
OMIM193200
Desc
Variant
Relatedalso


[PMID 21951294] A single nucleotide polymorphism rs9468925 of MHC region is associated with clinical features of generalized vitiligo in Chinese Han population


[PMID 20017995OA-icon.png] A principal-components-based clustering method to identify multiple variants associated with rheumatoid arthritis and arthritis-related autoantibodies.