rs7800244
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7800244(G;G) |
Make rs7800244(G;T) |
Make rs7800244(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 47740371 |
is a | snp |
is | mentioned by |
dbSNP | rs7800244 |
dbSNP (classic) | rs7800244 |
ClinGen | rs7800244 |
ebi | rs7800244 |
HLI | rs7800244 |
Exac | rs7800244 |
Gnomad | rs7800244 |
Varsome | rs7800244 |
LitVar | rs7800244 |
Map | rs7800244 |
PheGenI | rs7800244 |
Biobank | rs7800244 |
1000 genomes | rs7800244 |
hgdp | rs7800244 |
ensembl | rs7800244 |
geneview | rs7800244 |
scholar | rs7800244 |
rs7800244 | |
pharmgkb | rs7800244 |
gwascentral | rs7800244 |
openSNP | rs7800244 |
23andMe | rs7800244 |
SNPshot | rs7800244 |
SNPdbe | rs7800244 |
MSV3d | rs7800244 |
GWAS Ctlg | rs7800244 |
GMAF | 0.157 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22841784![]() |
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 |