rs9676717
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9676717(C;C) |
Make rs9676717(C;T) |
Make rs9676717(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 39187438 |
is a | snp |
is | mentioned by |
dbSNP | rs9676717 |
dbSNP (classic) | rs9676717 |
ClinGen | rs9676717 |
ebi | rs9676717 |
HLI | rs9676717 |
Exac | rs9676717 |
Gnomad | rs9676717 |
Varsome | rs9676717 |
LitVar | rs9676717 |
Map | rs9676717 |
PheGenI | rs9676717 |
Biobank | rs9676717 |
1000 genomes | rs9676717 |
hgdp | rs9676717 |
ensembl | rs9676717 |
geneview | rs9676717 |
scholar | rs9676717 |
rs9676717 | |
pharmgkb | rs9676717 |
gwascentral | rs9676717 |
openSNP | rs9676717 |
23andMe | rs9676717 |
SNPshot | rs9676717 |
SNPdbe | rs9676717 |
MSV3d | rs9676717 |
GWAS Ctlg | rs9676717 |
GMAF | 0.3792 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 23652058] Gene polymorphisms of interleukin-28, p21-activated protein kinases 4, and response to interferon-α based therapy in Chinese patients with chronic hepatitis B