ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.6177+1G>T

dbSNP: rs751142446
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnosis Center for Deafness RCV000770836 SCV001984926 pathogenic Autosomal recessive nonsyndromic hearing loss 3 criteria provided, single submitter clinical testing
Laboratory of Molecular Medicine, Institute of Maternal and Child Medicine, Affiliated Shenzhen Maternity & Child Healthcare Hospital, Southern Medical University RCV000770836 SCV004171060 pathogenic Autosomal recessive nonsyndromic hearing loss 3 criteria provided, single submitter clinical testing
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital RCV000770836 SCV000902337 likely pathogenic Autosomal recessive nonsyndromic hearing loss 3 2019-02-26 no assertion criteria provided case-control

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