LGALS14, galectin 14, 56891

N. diseases: 35; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs866674368
rs866674368
Entrez Id: 56891
Gene Symbol: LGALS14
LGALS14
CUI: C1384514
Disease:
Conn Syndrome 		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