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rs2273017

From SNPedia

Orientationminus
Stabilizedminus
Make rs2273017(C;C)
Make rs2273017(C;T)
Make rs2273017(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32369853
GeneC6orf10, LOC101929163
is asnp
is mentioned by
dbSNPrs2273017
dbSNP (classic)rs2273017
ClinGenrs2273017
ebirs2273017
HLIrs2273017
Exacrs2273017
Gnomadrs2273017
Varsomers2273017
LitVarrs2273017
Maprs2273017
PheGenIrs2273017
Biobankrs2273017
1000 genomesrs2273017
hgdprs2273017
ensemblrs2273017
geneviewrs2273017
scholarrs2273017
googlers2273017
pharmgkbrs2273017
gwascentralrs2273017
openSNPrs2273017
23andMers2273017
SNPshotrs2273017
SNPdbers2273017
MSV3drs2273017
GWAS Ctlgrs2273017
GMAF0.4826
Max Magnitude0
? (C;C) (C;T) (T;T) 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 A
P-val 2E-22
Odds Ratio 1.5300 [1.40-1.66]