ClinVar Miner

Submissions for variant NM_003356.4(UCP3):c.63C>G (p.Gly21=)

dbSNP: rs181883754
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001822273 SCV002066338 likely benign not specified 2018-02-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506846 SCV002810672 likely benign Obesity 2021-08-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002541963 SCV003251086 benign not provided 2022-10-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002541963 SCV005219489 likely benign not provided criteria provided, single submitter not provided

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