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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PQBP1
(R147* +1 more)
Single nucleotide variant
(nonsense +1 more)
Inborn genetic diseases
+1 more
GLikely pathogenic
AMER1, AMMECR1
+541 more
Indel
Heterotaxy, visceral, 1, X-linked
GPathogenic