Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs73982299
rs73982299
0.010 GeneticVariation BEFREE We identified two different de novo missense changes (p.Arg207His and p.Tyr679Cys) in <i>SLC12A6</i> in three unrelated individuals with early-onset progressive CMT. 31439721

2020