Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs866674368
rs866674368
LGALS14
0.010 GeneticVariation BEFREE We performed whole-exome sequencing in patients with early-onset primary aldosteronism and identified a de novo heterozygous c.71G>A/p.Gly24Asp mutation in the CLCN2 gene, encoding the voltage-gated ClC-2 chloride channel <sup>1</sup> , in a patient diagnosed at 9 years of age. 29403012

2018