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rs2236313

From SNPedia

Orientationplus
Stabilizedplus
Make rs2236313(C;C)
Make rs2236313(C;T)
Make rs2236313(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position166946901
GeneRNASET2
is asnp
is mentioned by
dbSNPrs2236313
ebirs2236313
HLIrs2236313
Exacrs2236313
Varsomers2236313
Maprs2236313
PheGenIrs2236313
hapmaprs2236313
1000 genomesrs2236313
hgdprs2236313
ensemblrs2236313
gopubmedrs2236313
geneviewrs2236313
scholarrs2236313
googlers2236313
pharmgkbrs2236313
gwascentralrs2236313
openSNPrs2236313
23andMers2236313
23andMe allrs2236313
SNP Nexus

SNPshotrs2236313
SNPdbers2236313
MSV3drs2236313
GWAS Ctlgrs2236313
GMAF0.4385
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 1E-16
Odds Ratio 1.20 [1.15-1.25]
OMIM193200
Desc
Variant
Relatedalso
Generalized Vitiligo


[PMID 22922229OA-icon.png] Seven newly identified loci for autoimmune thyroid disease.