ClinVar Miner

Submissions for variant NM_000237.3(LPL):c.-283G>T

gnomAD frequency: 0.00790  dbSNP: rs80351041
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000288145 SCV000472741 uncertain significance Hyperlipoproteinemia, type I 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001545856 SCV001765266 likely benign not provided 2019-05-04 criteria provided, single submitter clinical testing
Natera, Inc. RCV000288145 SCV002083198 benign Hyperlipoproteinemia, type I 2019-10-18 no assertion criteria provided clinical testing

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