List of variants in gene NOS3 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000603.5(NOS3):c.2984+15A>G	rs891512	0.85115
NM_000603.5(NOS3):c.894T>G (p.Asp298Glu)	rs1799983	0.76319
NM_000603.5(NOS3):c.774T>C (p.Asp258=)	rs1549758	0.75948
NM_000603.5(NOS3):c.1752+899G>A	rs79467411	0.10130
NM_000603.5(NOS3):c.1998C>G (p.Ala666=)	rs2566514

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