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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HERC2
(R2129C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
HERC2
Single nucleotide variant
(intron variant)
Developmental delay with autism spectrum disorder and gait instability
GUncertain significance