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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC20A2
(M645V)
Single nucleotide variant
(missense variant)
Idiopathic basal ganglia calcification 1
GUncertain significance
SLC20A2
(S601L)
Single nucleotide variant
(missense variant)
Idiopathic basal ganglia calcification 1
GPathogenic
SLC20A2
(A480fs)
Deletion
(frameshift variant)
Idiopathic basal ganglia calcification 1
GPathogenic
SLC20A2
(P286R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
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