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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP2B1
(M707I +7 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder, autosomal dominant 66
GUncertain significance
ATP2B1
(I199T +6 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder, autosomal dominant 66
GUncertain significance