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rs568406

From SNPedia

Orientationminus
Make rs568406(C;C)
Make rs568406(C;G)
Make rs568406(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position165924036
is asnp
is mentioned by
dbSNPrs568406
ebirs568406
HLIrs568406
Exacrs568406
Varsomers568406
Maprs568406
PheGenIrs568406
hapmaprs568406
1000 genomesrs568406
hgdprs568406
ensemblrs568406
gopubmedrs568406
geneviewrs568406
scholarrs568406
googlers568406
pharmgkbrs568406
gwascentralrs568406
openSNPrs568406
23andMers568406
23andMe allrs568406
SNP Nexus

SNPshotrs568406
SNPdbers568406
MSV3drs568406
GWAS Ctlgrs568406
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 26631030] Genetic variants in IL12 influence both hepatitis B virus clearance and HBV-related hepatocellular carcinoma development in a Chinese male population.