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rs4766578

From SNPedia

Orientationplus
Stabilizedplus
Make rs4766578(A;A)
Make rs4766578(A;T)
Make rs4766578(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position111466567
GeneATXN2
is asnp
is mentioned by
dbSNPrs4766578
ebirs4766578
HLIrs4766578
Exacrs4766578
Varsomers4766578
Maprs4766578
PheGenIrs4766578
hapmaprs4766578
1000 genomesrs4766578
hgdprs4766578
ensemblrs4766578
gopubmedrs4766578
geneviewrs4766578
scholarrs4766578
googlers4766578
pharmgkbrs4766578
gwascentralrs4766578
openSNPrs4766578
23andMers4766578
23andMe allrs4766578
SNP Nexus

SNPshotrs4766578
SNPdbers4766578
MSV3drs4766578
GWAS Ctlgrs4766578
GMAF0.2259
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 22561518OA-icon.png]
Trait
Title Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.
Risk Allele T
P-val 4E-18
Odds Ratio 1.3200 None