ClinVar Miner

Submissions for variant NM_003839.4(TNFRSF11A):c.75+5G>A

gnomAD frequency: 0.02406  dbSNP: rs146553439
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000173309 SCV000224408 benign not specified 2018-05-08 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000372728 SCV000410001 likely benign Bone Paget disease 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000278264 SCV000410002 likely benign Osteopetrosis 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001518769 SCV001727526 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001518769 SCV005207012 likely benign not provided criteria provided, single submitter not provided

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