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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANKRD17
Single nucleotide variant
(splice donor variant)
Chopra-Amiel-Gordon syndrome
GUncertain significance
ANKRD17
(P645S +1 more)
Single nucleotide variant
(missense variant)
Chopra-Amiel-Gordon syndrome
GUncertain significance