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rs7800244

From SNPedia

Orientationplus
Stabilizedplus
Make rs7800244(G;G)
Make rs7800244(G;T)
Make rs7800244(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position47740371
is asnp
is mentioned by
dbSNPrs7800244
ebirs7800244
HLIrs7800244
Exacrs7800244
Varsomers7800244
Maprs7800244
PheGenIrs7800244
hapmaprs7800244
1000 genomesrs7800244
hgdprs7800244
ensemblrs7800244
gopubmedrs7800244
geneviewrs7800244
scholarrs7800244
googlers7800244
pharmgkbrs7800244
gwascentralrs7800244
openSNPrs7800244
23andMers7800244
23andMe allrs7800244
SNP Nexus

SNPshotrs7800244
SNPdbers7800244
MSV3drs7800244
GWAS Ctlgrs7800244
GMAF0.157
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22841784OA-icon.png]
Trait Hepatitis C induced liver fibrosis
Title Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
Risk Allele T
P-val 3E-6
Odds Ratio NR NR