ClinVar Miner

Submissions for variant NM_002335.4(LRP5):c.488+11dup

gnomAD frequency: 0.00016  dbSNP: rs771667608
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002145456 SCV002421213 likely benign not provided 2023-12-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002508047 SCV002804854 likely benign Bone mineral density quantitative trait locus 1; Exudative vitreoretinopathy 4; Exudative vitreoretinopathy 1; Worth disease; Autosomal dominant osteopetrosis 1; Osteoporosis with pseudoglioma; Osteoporosis; Polycystic liver disease 4 with or without kidney cysts 2021-12-28 criteria provided, single submitter clinical testing

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