Related gene-specific medical variations for Gene (Select 124625862) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 877358	NM_022370.4(ROBO3):c.2515C>A (p.Leu839Ile)	LOC124625862, ROBO3 (L839I)	Single nucleotide variant (missense variant)	Gaze palsy, familial horizontal, with progressive scoliosis 1	GUncertain significance
Select item 733757	NM_022370.4(ROBO3):c.2472A>T (p.Ala824=)	LOC124625862, ROBO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 722199	NM_022370.4(ROBO3):c.2550C>T (p.Ser850=)	LOC124625862, ROBO3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 716324	NM_022370.4(ROBO3):c.2472A>C (p.Ala824=)	LOC124625862, ROBO3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 303254	NM_022370.4(ROBO3):c.2511C>G (p.Pro837=)	LOC124625862, ROBO3	Single nucleotide variant (synonymous variant)	Gaze palsy, familial horizontal, with progressive scoliosis 1	GUncertain significance
Select item 303253	NM_022370.4(ROBO3):c.2504T>C (p.Leu835Pro)	LOC124625862, ROBO3 (L835P)	Single nucleotide variant (missense variant)	Gaze palsy, familial horizontal, with progressive scoliosis 1	GUncertain significance

ClinVar