ClinVar Miner

Submissions for variant NM_001159699.2(FHL1):c.737-8C>A

dbSNP: rs2076705
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002082596 SCV002322670 likely benign X-linked myopathy with postural muscle atrophy 2022-05-12 criteria provided, single submitter clinical testing

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