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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMC1A
(Q1013H +1 more)
Single nucleotide variant
(missense variant)
Congenital muscular hypertrophy-cerebral syndrome
GUncertain significance
SMC1A
(Q588R +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SMC1A
Single nucleotide variant
(splice acceptor variant)
Congenital muscular hypertrophy-cerebral syndrome
GPathogenic
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