ClinVar Miner

Submissions for variant NM_017654.4(SAMD9):c.1645G>T (p.Val549Leu)

dbSNP: rs10279499
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001513796 SCV001721479 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001513796 SCV001851836 benign not provided 2019-06-15 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001513796 SCV002049303 benign not provided 2024-10-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001513796 SCV005268745 benign not provided criteria provided, single submitter not provided

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