ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.2355G>A (p.Met785Ile)

dbSNP: rs373362974
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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 RCV002129793 SCV002405323 benign Achondrogenesis, type IA 2021-04-10 criteria provided, single submitter clinical testing

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