ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.210G>A (p.Arg70=)

dbSNP: rs1364966765
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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 RCV001450787 SCV001654404 likely benign Achondrogenesis, type IA 2018-10-30 criteria provided, single submitter clinical testing

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