ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.1527+7C>G

dbSNP: rs372704269
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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 RCV000891974 SCV001035827 likely benign Achondrogenesis, type IA 2024-10-08 criteria provided, single submitter clinical testing

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