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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP24A1
(V218M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP24A1
(V158A)
Single nucleotide variant
(missense variant)
Hypercalcemia, infantile, 1
+2 more
GConflicting classifications of pathogenicity
CYP24A1
(T34M)
Single nucleotide variant
(missense variant)
Hypercalcemia, infantile, 1
+2 more
GUncertain significance
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