Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606914
rs267606914
0.700 GeneticVariation UNIPROT A novel NKX2.6 mutation associated with congenital ventricular septal defect. 25380965

2015

dbSNP: rs267606914
rs267606914
0.700 GeneticVariation UNIPROT Conotruncal malformations and absent thymus due to a deleterious NKX2-6 mutation. 24421281

2014

dbSNP: rs267606914
rs267606914
0.700 GeneticVariation UNIPROT Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease. 25195019

2014

dbSNP: rs267606914
rs267606914
0.700 GeneticVariation UNIPROT Common arterial trunk associated with a homeodomain mutation of NKX2.6. 15649947

2005