STX12, syntaxin 12, 23673

N. diseases: 6; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80194822
rs80194822
Entrez Id: 23673
Gene Symbol: STX12
STX12
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6598902
rs6598902
Entrez Id: 23673
Gene Symbol: STX12
STX12
CUI: C0947622
Disease:
Cholecystolithiasis 		0.700 GeneticVariation GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
dbSNP: rs6598902
rs6598902
Entrez Id: 23673
Gene Symbol: STX12
STX12
CUI: C0008350
Disease:
Cholelithiasis 		0.700 GeneticVariation GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007