ClinVar Miner

Submissions for variant NM_000603.5(NOS3):c.465C>G (p.Ala155=)

gnomAD frequency: 0.00080  dbSNP: rs200774720
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000939761 SCV001085612 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002489260 SCV002795078 likely benign Ischemic stroke; Alzheimer disease type 1; Preeclampsia/eclampsia 1; Essential hypertension, genetic 2021-10-08 criteria provided, single submitter clinical testing

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