ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.6354+35G>A

gnomAD frequency: 0.25401  dbSNP: rs3819170
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001533377 SCV001749255 benign Autosomal dominant nonsyndromic hearing loss 11 2021-07-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001533378 SCV001749256 likely benign Autosomal recessive nonsyndromic hearing loss 2 2021-07-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001533379 SCV001749257 likely benign Usher syndrome type 1 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001619946 SCV001844983 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001619946 SCV005214385 likely benign not provided criteria provided, single submitter not provided

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