ClinVar Miner

Submissions for variant NM_005450.6(NOG):c.582G>A (p.Pro194=)

gnomAD frequency: 0.00681  dbSNP: rs76347008
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000949824 SCV001096095 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000949824 SCV001780007 likely benign not provided 2020-10-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000949824 SCV005211091 likely benign not provided criteria provided, single submitter not provided

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