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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CASR
(W70*)
Single nucleotide variant
(nonsense)
Familial hypocalciuric hypercalcemia
+1 more
GPathogenic
CASR
(V165G)
Single nucleotide variant
(missense variant)
Familial hypocalciuric hypercalcemia
+3 more
GUncertain significance
CASR
(I760F +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
CASR
(S997Y +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant hypocalcemia 1
+1 more
GUncertain significance
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