ClinVar Miner

Submissions for variant NM_148897.3(SDR9C7):c.55C>G (p.Leu19Val)

gnomAD frequency: 0.00661  dbSNP: rs74397593
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Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002194311 SCV002482620 benign not provided 2024-10-28 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002222761 SCV002500493 likely benign not specified 2022-03-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002194311 SCV005215457 likely benign not provided criteria provided, single submitter not provided

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