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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAB3GAP2
(L174V)
Single nucleotide variant
(missense variant)
Martsolf syndrome
+1 more
GUncertain significance
RAB3GAP2
(S4P)
Single nucleotide variant
(missense variant)
Microcephaly
GUncertain significance