ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.6325A>C (p.Thr2109Pro)

dbSNP: rs2135791193
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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 RCV002051751 SCV001949933 uncertain significance Autosomal recessive nonsyndromic hearing loss 2 no assertion criteria provided case-control

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