ClinVar Miner

Submissions for variant NM_001008537.3(NEXMIF):c.1824A>G (p.Gln608=)

gnomAD frequency: 0.00001  dbSNP: rs758569887
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001720232 SCV000526365 likely benign not provided 2019-08-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001720232 SCV005784384 likely benign not provided 2024-04-10 criteria provided, single submitter clinical testing

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