ClinVar Miner

Submissions for variant NM_025207.5(FLAD1):c.1119G>A (p.Gly373=)

gnomAD frequency: 0.00083  dbSNP: rs142224458
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000967807 SCV000531108 likely benign not provided 2019-06-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000967807 SCV001115227 benign not provided 2024-01-11 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000967807 SCV001147440 uncertain significance not provided 2018-11-01 criteria provided, single submitter clinical testing

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