ClinVar Miner

Submissions for variant NM_001292063.2(OTOG):c.6405C>T (p.Thr2135=)

gnomAD frequency: 0.00007  dbSNP: rs187255209
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000733964 SCV000862072 uncertain significance not provided 2018-06-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000733964 SCV002433224 likely benign not provided 2024-10-24 criteria provided, single submitter clinical testing

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