rs9400317
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common on affy axiom data |
Make rs9400317(A;A) |
Make rs9400317(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 109686444 |
Gene | AK9 |
is a | snp |
is | mentioned by |
dbSNP | rs9400317 |
dbSNP (classic) | rs9400317 |
ClinGen | rs9400317 |
ebi | rs9400317 |
HLI | rs9400317 |
Exac | rs9400317 |
Gnomad | rs9400317 |
Varsome | rs9400317 |
LitVar | rs9400317 |
Map | rs9400317 |
PheGenI | rs9400317 |
Biobank | rs9400317 |
1000 genomes | rs9400317 |
hgdp | rs9400317 |
ensembl | rs9400317 |
geneview | rs9400317 |
scholar | rs9400317 |
rs9400317 | |
pharmgkb | rs9400317 |
gwascentral | rs9400317 |
openSNP | rs9400317 |
23andMe | rs9400317 |
SNPshot | rs9400317 |
SNPdbe | rs9400317 |
MSV3d | rs9400317 |
GWAS Ctlg | rs9400317 |
GMAF | 0.05923 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19684573] |
Trait | Response to Hepatitis C treatment |
Title | Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance |
Risk Allele | |
P-val | 0.000007 |
Odds Ratio | NR NR |