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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAB3GAP1
(G179A)
Single nucleotide variant
(missense variant)
Martsolf syndrome 2
GUncertain significance
RAB3GAP1
(R392*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
RAB3GAP1
(W481fs)
Microsatellite
(frameshift variant)
Warburg micro syndrome 1
GPathogenic
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