ClinVar Miner

Submissions for variant NM_000237.3(LPL):c.487C>T (p.His163Tyr)

dbSNP: rs2069951773
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001332299 SCV001524565 uncertain significance Hyperlipoproteinemia, type I 2019-07-16 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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