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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRPV6
(D324N)
Single nucleotide variant
(missense variant)
Hyperparathyroidism, transient neonatal
GUncertain significance
TRPV6
(R179fs)
Duplication
(frameshift variant)
not provided
+1 more
GPathogenic