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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AP1G1
(R416* +1 more)
Single nucleotide variant
(nonsense)
Usmani-Riazuddin syndrome, autosomal dominant
GPathogenic
AP1G1
(R15W)
Single nucleotide variant
(missense variant)
Usmani-Riazuddin syndrome, autosomal dominant
GLikely pathogenic