ClinVar Miner

Submissions for variant NM_144672.4(OTOA):c.121-20G>A

gnomAD frequency: 0.00516  dbSNP: rs7187792
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001593851 SCV001824162 likely benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001593851 SCV002328617 benign not provided 2024-11-11 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003120644 SCV003800278 benign Autosomal recessive nonsyndromic hearing loss 22 2022-07-15 criteria provided, single submitter clinical testing

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