ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.2905-162T>G

gnomAD frequency: 0.48946  dbSNP: rs59698916
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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 RCV001533335 SCV001749190 benign Autosomal dominant nonsyndromic hearing loss 11 2021-07-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001533336 SCV001749191 benign Autosomal recessive nonsyndromic hearing loss 2 2021-07-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001533337 SCV001749192 benign Usher syndrome type 1 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001647369 SCV001856174 benign not provided 2019-08-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001647369 SCV005236395 benign not provided criteria provided, single submitter not provided

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