"Ambry Genetics"[submitter] AND "LOC126860224"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3201325	NM_000603.5(NOS3):c.1252G>A (p.Val418Met)	LOC126860224, NOS3 (V418M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3201326	NM_000603.5(NOS3):c.1271C>T (p.Thr424Met)	LOC126860224, NOS3 (T424M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602249	NM_000603.5(NOS3):c.1421G>A (p.Arg474His)	LOC126860224, NOS3 (R474H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490248	NM_000603.5(NOS3):c.1463C>T (p.Thr488Ile)	LOC126860224, NOS3 (T488I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276743	NM_000603.5(NOS3):c.1507G>A (p.Val503Met)	LOC126860224, NOS3 (V503M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323587	NM_000603.5(NOS3):c.1559C>T (p.Ala520Val)	LOC126860224, NOS3 (A520V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar