ClinVar Miner

Submissions for variant NM_012210.4(TRIM32):c.6T>G (p.Ala2=)

gnomAD frequency: 0.00086  dbSNP: rs141352486
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000725427 SCV000336865 uncertain significance not provided 2017-05-02 criteria provided, single submitter clinical testing
GeneDx RCV000725427 SCV000530034 likely benign not provided 2021-03-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001088595 SCV000562342 benign Bardet-Biedl syndrome 2024-01-30 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV003151008 SCV003840140 likely benign not specified 2022-07-20 no assertion criteria provided clinical testing

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