ClinVar Miner

Submissions for variant NM_000255.4(MMUT):c.865A>C (p.Arg289=)

dbSNP: rs776371056
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001465054 SCV001669037 likely benign not provided 2023-01-16 criteria provided, single submitter clinical testing

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