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rs2069709

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2069709(G;T)
Make rs2069709(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position68159923
GeneIFNG
is asnp
is mentioned by
dbSNPrs2069709
ClinGenrs2069709
ebirs2069709
HLIrs2069709
Exacrs2069709
Varsomers2069709
Maprs2069709
PheGenIrs2069709
hapmaprs2069709
1000 genomesrs2069709
hgdprs2069709
ensemblrs2069709
gopubmedrs2069709
geneviewrs2069709
scholarrs2069709
googlers2069709
pharmgkbrs2069709
gwascentralrs2069709
openSNPrs2069709
23andMers2069709
23andMe allrs2069709
SNP Nexus

SNPshotrs2069709
SNPdbers2069709
MSV3drs2069709
GWAS Ctlgrs2069709
GMAF0.007805
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 20939703] The Interleukin 6 -572 G>C (rs1800796) Polymorphism Is Associated with the Risk of Developing Acute Coronary Syndrome


[PMID 17136124OA-icon.png] IFNG and IFNGR1 gene polymorphisms and susceptibility to post-kala-azar dermal leishmaniasis in Sudan.