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rs4678680

From SNPedia

Orientationplus
Stabilizedplus
Make rs4678680(G;G)
Make rs4678680(G;T)
Make rs4678680(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position32978543
is asnp
is mentioned by
dbSNPrs4678680
ebirs4678680
HLIrs4678680
Exacrs4678680
Varsomers4678680
Maprs4678680
PheGenIrs4678680
hapmaprs4678680
1000 genomesrs4678680
hgdprs4678680
ensemblrs4678680
gopubmedrs4678680
geneviewrs4678680
scholarrs4678680
googlers4678680
pharmgkbrs4678680
gwascentralrs4678680
openSNPrs4678680
23andMers4678680
23andMe allrs4678680
SNP Nexus

SNPshotrs4678680
SNPdbers4678680
MSV3drs4678680
GWAS Ctlgrs4678680
GMAF0.2351
Max Magnitude
? (G;G) (G;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 2E-7
Odds Ratio 2.2700 [1.68-3.08]


[PMID 27489354] Association of the GLB1 rs4678680 genetic variant with risk of HBV-related hepatocellular carcinoma.