ClinVar Miner

Submissions for variant NM_002524.5(NRAS):c.531G>A (p.Gly177=)

gnomAD frequency: 0.00001  dbSNP: rs1430947551
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001410060 SCV001612102 likely benign RASopathy 2019-02-18 criteria provided, single submitter clinical testing

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