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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CIROP
(Y68C)
Single nucleotide variant
(missense variant)
Heterotaxy, visceral, 12, autosomal
GUncertain significance
CIROP
(R22*)
Single nucleotide variant
(nonsense)
Heterotaxy, visceral, 12, autosomal
GUncertain significance