Have questions? Visit https://www.reddit.com/r/SNPedia

rs638893

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 1.22x risk of vitiligo in Chinese
(C;T) 1.22x risk of vitiligo in Chinese
(T;T) normal
ReferenceGRCh38 38.1/141
Chromosome11
Position118827828
is asnp
is mentioned by
dbSNPrs638893
ebirs638893
HLIrs638893
Exacrs638893
Varsomers638893
Maprs638893
PheGenIrs638893
hapmaprs638893
1000 genomesrs638893
hgdprs638893
ensemblrs638893
gopubmedrs638893
geneviewrs638893
scholarrs638893
googlers638893
pharmgkbrs638893
gwascentralrs638893
openSNPrs638893
23andMers638893
23andMe allrs638893
SNP Nexus

SNPshotrs638893
SNPdbers638893
MSV3drs638893
GWAS Ctlgrs638893
GMAF0.2048
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22951725]
Trait Vitiligo
Title Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population.
Risk Allele C
P-val 2E-9
Odds Ratio 1.22 [1.14-1.30]


[PMID 24001599] Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians