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rs117026326

From SNPedia

Orientationplus
Stabilizedplus
Make rs117026326(C;C)
Make rs117026326(C;T)
Make rs117026326(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position74711703
GeneGTF2I
is asnp
is mentioned by
dbSNPrs117026326
ebirs117026326
HLIrs117026326
Exacrs117026326
Varsomers117026326
Maprs117026326
PheGenIrs117026326
hapmaprs117026326
1000 genomesrs117026326
hgdprs117026326
ensemblrs117026326
gopubmedrs117026326
geneviewrs117026326
scholarrs117026326
googlers117026326
pharmgkbrs117026326
gwascentralrs117026326
openSNPrs117026326
23andMers117026326
23andMe allrs117026326
SNP Nexus

SNPshotrs117026326
SNPdbers117026326
MSV3drs117026326
GWAS Ctlgrs117026326
GMAF0.03168
Max Magnitude

[PMID 24097066] A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23

[PMID 25480810] The GTF2I rs117026326 polymorphism is associated with anti-SSA-positive primary Sjögren's syndrome