Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs117026326
rs117026326
Entrez Id: 2969;101926943
Gene Symbol: GTF2I;LOC101926943
GTF2I;LOC101926943
CUI: C0151449
Disease:
Primary Sjögren's syndrome
0.020 GeneticVariation BEFREE Genetic variant rs117026326 upstream of the general transcription factor II-I (GTF2I) has been associated with primary Sjögren's syndrome, SLE and RA in East Asian populations. 31520790 2019
dbSNP: rs117026326
rs117026326
Entrez Id: 2969;101926943
Gene Symbol: GTF2I;LOC101926943
GTF2I;LOC101926943
CUI: C0151449
Disease:
Primary Sjögren's syndrome
0.020 GeneticVariation BEFREE The combined analysis identified GTF2I at 7q11.23 (rs117026326: Pcombined = 1.31 × 10(-53), combined odds ratio (ORcombined) = 2.20) as a new susceptibility locus for primary Sjögren's syndrome. 24097066 2013