ClinVar Miner

Submissions for variant NM_001302998.2(LIPI):c.164G>A (p.Cys55Tyr)

gnomAD frequency: 0.00748  dbSNP: rs11909217
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002054409 SCV002385147 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002054409 SCV005307096 benign not provided criteria provided, single submitter not provided
OMIM RCV001851568 SCV000022052 uncertain significance Hypertriglyceridemia 1 2003-05-15 no assertion criteria provided literature only

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