ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.5473G>A (p.Val1825Met)

gnomAD frequency: 0.00008  dbSNP: rs368883957
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002000715 SCV002267727 likely benign not provided 2024-09-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002479654 SCV002794000 uncertain significance Autosomal recessive nonsyndromic hearing loss 3 2021-07-02 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002000715 SCV005192771 uncertain significance not provided criteria provided, single submitter not provided

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