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rs4908760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 0 common in complete genomics
Make rs4908760(A;A)
Make rs4908760(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position8466082
GeneRERE
is asnp
is mentioned by
dbSNPrs4908760
ebirs4908760
HLIrs4908760
Exacrs4908760
Varsomers4908760
Maprs4908760
PheGenIrs4908760
hapmaprs4908760
1000 genomesrs4908760
hgdprs4908760
ensemblrs4908760
gopubmedrs4908760
geneviewrs4908760
scholarrs4908760
googlers4908760
pharmgkbrs4908760
gwascentralrs4908760
openSNPrs4908760
23andMers4908760
23andMe allrs4908760
SNP Nexus

SNPshotrs4908760
SNPdbers4908760
MSV3drs4908760
GWAS Ctlgrs4908760
GMAF0.281
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20410501OA-icon.png]
Trait Vitiligo
Title Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo
Risk Allele G
P-val 7E-15
Odds Ratio 1.36 [1.26-1.48]