C1838625[trait identifier] AND "Department Of Genetics, Sultan Qaboos - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 545410	NM_012233.3(RAB3GAP1):c.1039C>T (p.Arg347Ter)	RAB3GAP1 (R347*)	Single nucleotide variant (nonsense)	not provided +2 more	GPathogenic
Select item 623318	NM_012233.3(RAB3GAP1):c.1237-2A>G	RAB3GAP1	Single nucleotide variant (splice acceptor variant)	Warburg micro syndrome 1	GPathogenic
Select item 623319	NM_012233.3(RAB3GAP1):c.2491G>T (p.Glu831Ter)	RAB3GAP1 (E831*)	Single nucleotide variant (nonsense)	Warburg micro syndrome 1	GPathogenic

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