ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.7743G>T (p.Thr2581=)

gnomAD frequency: 0.00015  dbSNP: rs140698184
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 RCV000880209 SCV001023289 likely benign not provided 2024-01-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501371 SCV002808101 likely benign Donnai-Barrow syndrome 2021-12-15 criteria provided, single submitter clinical testing

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