ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.5133+26A>C

dbSNP: rs2075658
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001660785 SCV001873134 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001779287 SCV002015851 benign Autosomal recessive nonsyndromic hearing loss 3 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001660785 SCV005248566 benign not provided criteria provided, single submitter not provided

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