ClinVar Miner

Submissions for variant NM_001159699.2(FHL1):c.737-10T>C

gnomAD frequency: 0.00004  dbSNP: rs767421819
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001452374 SCV001656034 likely benign X-linked myopathy with postural muscle atrophy 2024-12-15 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004800506 SCV005423116 likely benign not specified 2024-10-06 criteria provided, single submitter clinical testing

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