SLC12A3, solute carrier family 12 member 3, 6559

N. diseases: 252; N. variants: 131
Disease: Gitelman Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs559626481
rs559626481
Entrez Id: 6559;102466752
Gene Symbol: SLC12A3;MIR6863
SLC12A3;MIR6863
CUI: C0268450
Disease:
Gitelman Syndrome 		T 0.700 GeneticVariation CLINVAR Spectrum of mutations in Gitelman syndrome. 21415153 2011