Related gene-specific medical variations for Gene (Select 285282) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312244	NM_173825.5(RABL3):c.7T>A (p.Ser3Thr)	LOC112872291, RABL3 (S3T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3150944	NM_173825.5(RABL3):c.20T>G (p.Val7Gly)	LOC112872291, RABL3 (V7G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3051382	NM_173825.5(RABL3):c.46+6C>T	LOC112872291, RABL3	Single nucleotide variant (intron variant)	RABL3-related disorder	GLikely benign

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