ClinVar Miner

Submissions for variant NM_183381.3(RNF13):c.1073T>C (p.Ile358Thr)

dbSNP: rs769543244
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001996262 SCV002284592 likely benign not provided 2024-10-24 criteria provided, single submitter clinical testing

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