ClinVar Miner

Submissions for variant NM_001039213.4(CEACAM16):c.763A>G (p.Arg255Gly)

gnomAD frequency: 0.00001  dbSNP: rs1347137461
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ColIege of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital RCV001544499 SCV001762270 pathogenic Autosomal dominant nonsyndromic hearing loss 4B 2020-07-01 no assertion criteria provided case-control

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