Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.240 GeneticVariation BEFREE The KCNQ1 rs3864884 and rs12576239 genetic variants were associated with hypertension in T2DM. 28059450

2017
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.240 GeneticVariation BEFREE Therefore, our data support that KCNQ1 is associated with an increased risk for T2DM and might contribute to the higher incidence of hypertension and macrovascular complications in patients with T2DM carrying the risk allele C though it needs further to be confirmed in a larger population. 26678516

2015
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.240 GeneticVariation BEFREE Five single nucleotide polymorphisms (SNPs) near the protein tyrosine phosphatase, receptor type, D (PTPRD), SRR, MAF/WWOX, and KCNQ1 genes were genotyped in 1138 subjects of Chinese origin from the Stanford Asia-Pacific Program for Hypertension and Insulin Resistance study. 21767287

2012
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.240 GeneticVariation BEFREE One missense KCNQ1 mutation, R14C, was identified in 1 family with a high prevalence of hypertension. 17276182

2007