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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNA1
(V335F +1 more)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 1A
GUncertain significance
CHRNA1
(I100F +1 more)
Single nucleotide variant
(missense variant)
Lethal multiple pterygium syndrome
+1 more
GUncertain significance