SLC12A3, solute carrier family 12 member 3, 6559

N. diseases: 252; N. variants: 131
Disease: Hypomagnesemia ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs200817545
rs200817545 		0.925 0.160 16 56879168 missense variant A/C;G;T snv 4.0E-06; 1.6E-04
CUI: C0151723
Disease: Hypomagnesemia
Hypomagnesemia 		Nutritional and Metabolic Diseases 0.700 0