ClinVar Miner

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