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rs3893464

From SNPedia

Orientationminus
Stabilizedminus
Make rs3893464(C;C)
Make rs3893464(C;T)
Make rs3893464(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29967473
GeneHCG2P6
is asnp
is mentioned by
dbSNPrs3893464
ebirs3893464
HLIrs3893464
Exacrs3893464
Varsomers3893464
Maprs3893464
PheGenIrs3893464
hapmaprs3893464
1000 genomesrs3893464
hgdprs3893464
ensemblrs3893464
gopubmedrs3893464
geneviewrs3893464
scholarrs3893464
googlers3893464
pharmgkbrs3893464
gwascentralrs3893464
openSNPrs3893464
23andMers3893464
23andMe allrs3893464
SNP Nexus

SNPshotrs3893464
SNPdbers3893464
MSV3drs3893464
GWAS Ctlgrs3893464
GMAF0.4761
Max Magnitude
? (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 G
P-val 2E-20
Odds Ratio 1.5300 [1.39-1.67]