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rs1417210

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0.88x risk of vitiligo in Chinese
(C;T) 0.88x risk of vitiligo in Chinese
(T;T) normal
ReferenceGRCh38 38.1/142
Chromosome10
Position71376162
is asnp
is mentioned by
dbSNPrs1417210
ebirs1417210
HLIrs1417210
Exacrs1417210
Varsomers1417210
Maprs1417210
PheGenIrs1417210
hapmaprs1417210
1000 genomesrs1417210
hgdprs1417210
ensemblrs1417210
gopubmedrs1417210
geneviewrs1417210
scholarrs1417210
googlers1417210
pharmgkbrs1417210
gwascentralrs1417210
openSNPrs1417210
23andMers1417210
23andMe allrs1417210
SNP Nexus

SNPshotrs1417210
SNPdbers1417210
MSV3drs1417210
GWAS Ctlgrs1417210
GMAF0.1768
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
P-val 2E-8
Odds Ratio 1.14 [1.09-1.19]