ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.4368-7_4374del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005041229 SCV005675509 likely pathogenic Autosomal recessive nonsyndromic hearing loss 23; Usher syndrome type 1D; Usher syndrome type 1F 2024-03-15 criteria provided, single submitter clinical testing

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