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rs9366816

From SNPedia

Orientationplus
Stabilizedplus
Make rs9366816(C;C)
Make rs9366816(C;T)
Make rs9366816(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position33136398
is asnp
is mentioned by
dbSNPrs9366816
ebirs9366816
HLIrs9366816
Exacrs9366816
Varsomers9366816
Maprs9366816
PheGenIrs9366816
hapmaprs9366816
1000 genomesrs9366816
hgdprs9366816
ensemblrs9366816
gopubmedrs9366816
geneviewrs9366816
scholarrs9366816
googlers9366816
pharmgkbrs9366816
gwascentralrs9366816
openSNPrs9366816
23andMers9366816
23andMe allrs9366816
SNP Nexus

SNPshotrs9366816
SNPdbers9366816
MSV3drs9366816
GWAS Ctlgrs9366816
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24940741OA-icon.png]
Trait Chronic hepatitis B infection
Title A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese.
Risk Allele C
P-val 3E-10
Odds Ratio 1.43 [1.28-1.60]