ClinVar Miner

Submissions for variant NM_003839.4(TNFRSF11A):c.*634_*635dup

dbSNP: rs142942284
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000291400 SCV000410059 likely benign Bone Paget disease 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000320710 SCV000410060 likely benign Osteopetrosis 2016-06-14 criteria provided, single submitter clinical testing

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