ClinVar Miner

Submissions for variant NM_005379.4(MYO1A):c.2728T>C (p.Ser910Pro)

gnomAD frequency: 0.00001  dbSNP: rs121909306
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000008628 SCV000028836 uncertain significance Autosomal dominant nonsyndromic hearing loss 48 2014-05-01 no assertion criteria provided literature only

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