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rs9267673

From SNPedia

Orientationplus
Stabilizedplus
Make rs9267673(C;C)
Make rs9267673(C;T)
Make rs9267673(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31915902
GeneC2
is asnp
is mentioned by
dbSNPrs9267673
ebirs9267673
HLIrs9267673
Exacrs9267673
Varsomers9267673
Maprs9267673
PheGenIrs9267673
hapmaprs9267673
1000 genomesrs9267673
hgdprs9267673
ensemblrs9267673
gopubmedrs9267673
geneviewrs9267673
scholarrs9267673
googlers9267673
pharmgkbrs9267673
gwascentralrs9267673
openSNPrs9267673
23andMers9267673
23andMe allrs9267673
SNP Nexus

SNPshotrs9267673
SNPdbers9267673
MSV3drs9267673
GWAS Ctlgrs9267673
GMAF0.1217
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21105107]
Trait
Title Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma.
Risk Allele
P-val 0.000002
Odds Ratio 1.9700 [1.47-2.64]


[PMID 26538132OA-icon.png] Genetic variations in STAT4,C2,HLA-DRB1 and HLA-DQ associated with risk of hepatitis B virus-related liver cirrhosis