"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ADGRA2" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 716089	NM_032777.10(ADGRA2):c.1608+5T>C	ADGRA2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 775264	NM_032777.10(ADGRA2):c.2013G>A (p.Arg671=)	ADGRA2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 776318	NM_032777.10(ADGRA2):c.2041G>A (p.Ala681Thr)	ADGRA2 (A681T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 768235	NM_032777.10(ADGRA2):c.3046G>C (p.Gly1016Arg)	ADGRA2 (G1016R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2425692	NC_000008.10:g.(?_37595441)_(38961219_?)dup	ADAM9, ADGRA2 +21 more	Duplication	Spastic paraplegia +3 more	GUncertain significance
Select item 1455925	NC_000008.10:g.(?_37595441)_(38961219_?)del	ADAM9, ADGRA2 +21 more	Deletion	not provided	GPathogenic

ClinVar