ClinVar Miner

Submissions for variant NM_017837.4(PIGV):c.876A>G (p.Glu292=)

gnomAD frequency: 0.00002  dbSNP: rs756422269
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001550470 SCV001770801 likely benign not provided 2021-01-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001550470 SCV003239015 likely benign not provided 2024-10-17 criteria provided, single submitter clinical testing

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