ClinVar Miner

Submissions for variant NM_003839.4(TNFRSF11A):c.*1251dup

dbSNP: rs150401931
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
Illumina Laboratory Services, Illumina RCV000259433 SCV000410079 likely benign Bone Paget disease 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000317703 SCV000410080 likely benign Osteopetrosis 2016-06-14 criteria provided, single submitter clinical testing

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