Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs559626481
rs559626481
SLC12A3 ; MIR6863
CUI: C0268450
Disease: Gitelman Syndrome
Gitelman Syndrome 		T 0.700 GeneticVariation CLINVAR Spectrum of mutations in Gitelman syndrome. 21415153

2011