ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.9587ACA[1] (p.Asn3197del)

dbSNP: rs763993100
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001580653 SCV001810319 uncertain significance Autosomal recessive nonsyndromic hearing loss 12 2021-07-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001580652 SCV001810320 uncertain significance Usher syndrome type 1D 2021-07-22 criteria provided, single submitter clinical testing

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