Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777710
rs587777710
Entrez Id: 2627
Gene Symbol: GATA6
GATA6
CUI: C0235833
Disease:
Congenital diaphragmatic hernia
T 0.710 CausalMutation CLINVAR In the second, a nonsense mutation (c.712G>T, p.G238*) was identified in two siblings with CDH and a large ventricular septal defect. 24385578 2014
dbSNP: rs587777710
rs587777710
Entrez Id: 2627
Gene Symbol: GATA6
GATA6
CUI: C0235833
Disease:
Congenital diaphragmatic hernia
0.710 GeneticVariation BEFREE In the second, a nonsense mutation (c.712G>T, p.G238*) was identified in two siblings with CDH and a large ventricular septal defect. 24385578 2014