ClinVar Miner

Submissions for variant NM_001145308.5(LRTOMT):c.333C>G (p.Tyr111Ter)

dbSNP: rs137853188
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000000576 SCV000020725 pathogenic Autosomal recessive nonsyndromic hearing loss 63 2008-09-23 no assertion criteria provided literature only

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