ClinVar Miner

Submissions for variant NM_000895.3(LTA4H):c.1074G>A (p.Gly358=)

gnomAD frequency: 0.00135  dbSNP: rs147001898
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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 RCV000969078 SCV001116570 benign not provided 2018-07-26 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000969078 SCV004129734 likely benign not provided 2022-04-01 criteria provided, single submitter clinical testing LTA4H: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV000969078 SCV005234830 benign not provided criteria provided, single submitter not provided

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