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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PKD1L1
Deletion
(splice donor variant)
Heterotaxy, visceral, 8, autosomal
+2 more
GPathogenic
PKD1L1
(P676L)
Single nucleotide variant
(missense variant)
Heterotaxy, visceral, 8, autosomal
GUncertain significance