ClinVar Miner

Submissions for variant NM_002332.3(LRP1):c.1458G>A (p.Pro486=)

gnomAD frequency: 0.00040  dbSNP: rs138966453
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000903317 SCV001047778 benign not provided 2018-07-18 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000903317 SCV004133511 likely benign not provided 2022-08-01 criteria provided, single submitter clinical testing LRP1: BP4, BP7

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