ClinVar Miner

Submissions for variant NM_017433.5(MYO3A):c.732-2A>G

dbSNP: rs1023746725
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000004231 SCV000024397 pathogenic Autosomal recessive nonsyndromic hearing loss 30 2002-05-28 no assertion criteria provided literature only

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