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rs3997872

From SNPedia

Orientationplus
Make rs3997872(A;A)
Make rs3997872(A;T)
Make rs3997872(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position32612840
is asnp
is mentioned by
dbSNPrs3997872
ebirs3997872
HLIrs3997872
Exacrs3997872
Varsomers3997872
Maprs3997872
PheGenIrs3997872
hapmaprs3997872
1000 genomesrs3997872
hgdprs3997872
ensemblrs3997872
gopubmedrs3997872
geneviewrs3997872
scholarrs3997872
googlers3997872
pharmgkbrs3997872
gwascentralrs3997872
openSNPrs3997872
23andMers3997872
23andMe allrs3997872
SNP Nexus

SNPshotrs3997872
SNPdbers3997872
MSV3drs3997872
GWAS Ctlgrs3997872
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 26538132] Genetic variations in STAT4,C2,HLA-DRB1 and HLA-DQ associated with risk of hepatitis B virus-related liver cirrhosis