ClinVar Miner

Submissions for variant NM_144672.4(OTOA):c.*47A>G

gnomAD frequency: 0.37728  dbSNP: rs460598
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001661111 SCV001874388 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788709 SCV002029331 benign Autosomal recessive nonsyndromic hearing loss 22 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001661111 SCV005293120 benign not provided criteria provided, single submitter not provided

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