GTF2I, general transcription factor IIi, 2969

N. diseases: 249; N. variants: 14
Disease: Sjogren's Syndrome ×
Source: ALL
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: C1527336
Disease:
Sjogren's Syndrome 		T 0.800 GeneticVariation GWASCAT Identification of susceptibility gene associated with female primary Sjögren's syndrome in Han Chinese by genome-wide association study. 27503288 2016
dbSNP: rs117026326
rs117026326
Entrez Id: 2969;101926943
Gene Symbol: GTF2I;LOC101926943
GTF2I;LOC101926943
CUI: C1527336
Disease:
Sjogren's Syndrome 		T 0.800 GeneticVariation GWASCAT A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23. 24097066 2013
dbSNP: rs117026326
rs117026326
Entrez Id: 2969;101926943
Gene Symbol: GTF2I;LOC101926943
GTF2I;LOC101926943
CUI: C1527336
Disease:
Sjogren's Syndrome 		T 0.800 GeneticVariation GWASDB A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23. 24097066 2013