ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.93-15T>C

gnomAD frequency: 0.00001  dbSNP: rs35456885
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253363 SCV000304634 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003105837 SCV003781944 likely benign not provided 2024-02-22 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000253363 SCV004028775 uncertain significance not specified 2023-07-26 criteria provided, single submitter clinical testing

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