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rs2069710

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs2069710(A;G)
Make rs2069710(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position68159895
GeneIFNG
is asnp
is mentioned by
dbSNPrs2069710
ebirs2069710
HLIrs2069710
Exacrs2069710
Varsomers2069710
Maprs2069710
PheGenIrs2069710
hapmaprs2069710
1000 genomesrs2069710
hgdprs2069710
ensemblrs2069710
gopubmedrs2069710
geneviewrs2069710
scholarrs2069710
googlers2069710
pharmgkbrs2069710
gwascentralrs2069710
openSNPrs2069710
23andMers2069710
23andMe allrs2069710
SNP Nexus

SNPshotrs2069710
SNPdbers2069710
MSV3drs2069710
GWAS Ctlgrs2069710
GMAF0.0005
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 20939703] The Interleukin 6 -572 G>C (rs1800796) Polymorphism Is Associated with the Risk of Developing Acute Coronary Syndrome