"Invitae"[submitter] AND "LOC126806727"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1986878	NM_001395656.1(ROBO2):c.1984-10T>C	LOC126806727, ROBO2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 346696	NM_001395656.1(ROBO2):c.2030G>A (p.Arg677His)	LOC126806727, ROBO2 (R673H +6 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 1136675	NM_001395656.1(ROBO2):c.2051C>T (p.Ala684Val)	LOC126806727, ROBO2 (A680V +6 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1911741	NM_001395656.1(ROBO2):c.2061G>A (p.Ser687=)	LOC126806727, ROBO2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 346697	NM_001395656.1(ROBO2):c.2086C>T (p.Pro696Ser)	LOC126806727, ROBO2 (P692S +6 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2009453	NM_001395656.1(ROBO2):c.2196G>C (p.Thr732=)	LOC126806727, ROBO2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 744404	NM_001395656.1(ROBO2):c.2196G>A (p.Thr732=)	LOC126806727, ROBO2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2067223	NM_001395656.1(ROBO2):c.2201G>A (p.Arg734His)	LOC126806727, ROBO2 (R750H +6 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar