ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.6491del (p.Asn2164fs)

dbSNP: rs2135802675
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Deafness Molecular Diagnostic Center, Chinese PLA General Hospital RCV001823216 SCV001763655 likely pathogenic Autosomal recessive nonsyndromic hearing loss 2 no assertion criteria provided case-control

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