ClinVar Miner

Submissions for variant NM_173477.5(USH1G):c.1060G>T (p.Asp354Tyr)

dbSNP: rs1316299165
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital RCV000770886 SCV000902400 pathogenic Usher syndrome type 1G 2019-02-26 no assertion criteria provided case-control

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