ClinVar Miner

Submissions for variant NM_000078.3(CETP):c.268C>T (p.Gln90Ter)

dbSNP: rs2056091646
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001780486 SCV002017039 pathogenic Hyperalphalipoproteinemia 1 2019-09-24 criteria provided, single submitter clinical testing

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