ClinVar Miner

Submissions for variant NM_005219.5(DIAPH1):c.3661+16G>A

dbSNP: rs2154594915
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002125148 SCV002445006 likely benign Autosomal dominant nonsyndromic hearing loss 1; Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome 2023-11-07 criteria provided, single submitter clinical testing

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