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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GCM2
(S285fs)
Deletion
(frameshift variant)
Hypoparathyroidism, familial isolated, 2
GLikely pathogenic
GCM2
(L101V)
Single nucleotide variant
(missense variant)
Hypoparathyroidism, familial isolated, 2
GUncertain significance