ClinVar Miner

Submissions for variant NM_002335.4(LRP5):c.1299C>T (p.Thr433=)

gnomAD frequency: 0.00016  dbSNP: rs145362529
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000728311 SCV000855866 uncertain significance not provided 2017-08-03 criteria provided, single submitter clinical testing
Invitae RCV000728311 SCV001049350 likely benign not provided 2023-09-10 criteria provided, single submitter clinical testing
GeneDx RCV000728311 SCV001759457 likely benign not provided 2019-11-21 criteria provided, single submitter clinical testing

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