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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CASR
(R220W)
Single nucleotide variant
(missense variant)
Familial hypocalciuric hypercalcemia 1
+5 more
GPathogenic
CASR
(T686R +1 more)
Single nucleotide variant
(missense variant)
Familial hypocalciuric hypercalcemia
+5 more
GUncertain significance