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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMC1A
(Q1073* +1 more)
Single nucleotide variant
(nonsense)
Congenital muscular hypertrophy-cerebral syndrome
GPathogenic
SMC1A
(E243del +1 more)
Deletion
(inframe_deletion)
not provided
GConflicting classifications of pathogenicity