Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906653
rs387906653
SLC20A2
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
Idiopathic basal ganglia calcification 1 		T 0.800 GeneticVariation CLINVAR Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis. 22327515

2012
dbSNP: rs387906653
rs387906653
SLC20A2
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
Idiopathic basal ganglia calcification 1 		T 0.800 CausalMutation CLINVAR

dbSNP: rs387906653
rs387906653
SLC20A2
CUI: C4551624
Disease: Idiopathic basal ganglia calcification 1
Idiopathic basal ganglia calcification 1 		A 0.800 CausalMutation CLINVAR