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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HERC2
(V3614M)
Single nucleotide variant
(missense variant)
Developmental delay with autism spectrum disorder and gait instability
GUncertain significance
HERC2
(I1141V)
Single nucleotide variant
(missense variant)
Developmental delay with autism spectrum disorder and gait instability
GUncertain significance