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rs9676717

From SNPedia

Orientationplus
Stabilizedplus
Make rs9676717(C;C)
Make rs9676717(C;T)
Make rs9676717(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position39187438
is asnp
is mentioned by
dbSNPrs9676717
ebirs9676717
HLIrs9676717
Exacrs9676717
Varsomers9676717
Maprs9676717
PheGenIrs9676717
hapmaprs9676717
1000 genomesrs9676717
hgdprs9676717
ensemblrs9676717
gopubmedrs9676717
geneviewrs9676717
scholarrs9676717
googlers9676717
pharmgkbrs9676717
gwascentralrs9676717
openSNPrs9676717
23andMers9676717
23andMe allrs9676717
SNP Nexus

SNPshotrs9676717
SNPdbers9676717
MSV3drs9676717
GWAS Ctlgrs9676717
GMAF0.3792
Max Magnitude
? (C;C) (C;T) (T;T) 28

[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