C1838625[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 130064	NM_012233.3(RAB3GAP1):c.1793A>G (p.Asn598Ser)	RAB3GAP1 (N598S)	Single nucleotide variant (missense variant)	Warburg micro syndrome 1 +3 more	GBenign
Select item 130067	NM_012233.3(RAB3GAP1):c.2265T>C (p.Phe755=)	RAB3GAP1	Single nucleotide variant (synonymous variant)	Martsolf syndrome 2 +4 more	GBenign