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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD1A
(R217H)
Single nucleotide variant
(missense variant)
Autism
GUncertain significance
SETD1A
(C1638F)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance