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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CASR
(S810N +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant hypocalcemia 1
GPathogenic
CASR
(E127K)
Single nucleotide variant
(missense variant)
Nephrolithiasis/nephrocalcinosis
+5 more
GPathogenic/Likely pathogenic
CASR
(I822T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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