SLC20A2, solute carrier family 20 member 2, 6575

N. diseases: 104; N. variants: 36
Disease: Idiopathic basal ganglia calcification 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1563498184
rs1563498184
Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
CUI: C4551624
Disease:
Idiopathic basal ganglia calcification 1 		A 0.700 GeneticVariation CLINVAR