ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.133-88C>T

gnomAD frequency: 0.19502  dbSNP: rs12279716
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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 RCV001533387 SCV001749273 benign Autosomal dominant nonsyndromic hearing loss 11 2021-07-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001533388 SCV001749274 benign Autosomal recessive nonsyndromic hearing loss 2 2021-07-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001533389 SCV001749275 benign Usher syndrome type 1 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001615253 SCV001835920 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615253 SCV005235689 benign not provided criteria provided, single submitter not provided

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