SLC20A2, solute carrier family 20 member 2, 6575

N. diseases: 104; N. variants: 36
Disease: Idiopathic basal ganglia calcification 1 ×
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: rs387906654
rs387906654 		1.000 0.080 8 42428768 missense variant G/A snv
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
Idiopathic basal ganglia calcification 1 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.800 1.000 8 2005 2014