ClinVar Miner

Submissions for variant NM_017433.5(MYO3A):c.586-28A>G

gnomAD frequency: 0.06787  dbSNP: rs41314631
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001653226 SCV001871469 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001779297 SCV002015886 benign Autosomal recessive nonsyndromic hearing loss 30 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001653226 SCV005320583 benign not provided criteria provided, single submitter not provided

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