ClinVar Miner

Submissions for variant NM_001159699.2(FHL1):c.737-3dup

dbSNP: rs368428875
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003624204 SCV004518636 benign X-linked myopathy with postural muscle atrophy 2024-01-31 criteria provided, single submitter clinical testing

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