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rs3132613

From SNPedia

Orientationminus
Stabilizedminus
Make rs3132613(C;C)
Make rs3132613(C;G)
Make rs3132613(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position30569829
GeneABCF1, LOC107986587
is asnp
is mentioned by
dbSNPrs3132613
dbSNP (classic)rs3132613
ClinGenrs3132613
ebirs3132613
HLIrs3132613
Exacrs3132613
Gnomadrs3132613
Varsomers3132613
LitVarrs3132613
Maprs3132613
PheGenIrs3132613
Biobankrs3132613
1000 genomesrs3132613
hgdprs3132613
ensemblrs3132613
geneviewrs3132613
scholarrs3132613
googlers3132613
pharmgkbrs3132613
gwascentralrs3132613
openSNPrs3132613
23andMers3132613
SNPshotrs3132613
SNPdbers3132613
MSV3drs3132613
GWAS Ctlgrs3132613
GMAF0.2865
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 21900946]
Trait
Title Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
Risk Allele C
P-val 1E-13
Odds Ratio 1.4300 [1.30-1.57]