ClinVar Miner

Submissions for variant NM_001159699.2(FHL1):c.183G>A (p.Lys61=)

dbSNP: rs780792982
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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 RCV002128749 SCV002454403 likely benign X-linked myopathy with postural muscle atrophy 2021-01-14 criteria provided, single submitter clinical testing

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