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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP13A3
(M823fs +1 more)
Duplication
(frameshift variant +1 more)
Pulmonary hypertension, primary, autosomal recessive
+1 more
GPathogenic
ATP13A3
(R716C +1 more)
Single nucleotide variant
(missense variant +1 more)
Pulmonary hypertension, primary, autosomal recessive
+1 more
GLikely pathogenic