ClinVar (all) for Orgtrack (Select 506500) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 517660	NM_000603.5(NOS3):c.-51-762C>T	LOC110973015, NOS3	Single nucleotide variant (intron variant)	Metabolic syndrome, susceptibility to	Gprotective
Select item 496809	NM_000603.4(NOS3):c.[774T>C;894T>G]	NOS3 (D298E)	Single nucleotide variant (missense variant +1 more)	Metabolic syndrome, susceptibility to	Grisk factor