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rs12980602

From SNPedia

Orientationplus
Stabilizedplus
Make rs12980602(C;C)
Make rs12980602(C;T)
Make rs12980602(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position39262180
is asnp
is mentioned by
dbSNPrs12980602
ebirs12980602
HLIrs12980602
Exacrs12980602
Varsomers12980602
Maprs12980602
PheGenIrs12980602
hapmaprs12980602
1000 genomesrs12980602
hgdprs12980602
ensemblrs12980602
gopubmedrs12980602
geneviewrs12980602
scholarrs12980602
googlers12980602
pharmgkbrs12980602
gwascentralrs12980602
openSNPrs12980602
23andMers12980602
23andMe allrs12980602
SNP Nexus

SNPshotrs12980602
SNPdbers12980602
MSV3drs12980602
GWAS Ctlgrs12980602
GMAF0.2319
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


[PMID 23586360] Association between gene polymorphisms of IL-28 and response to lamivudine in Chinese rural patients with chronic hepatitis B.