ClinVar Miner

Submissions for variant NM_003839.4(TNFRSF11A):c.*320dup

dbSNP: rs552069161
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000348145 SCV000410043 uncertain significance Bone Paget disease 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000400681 SCV000410044 uncertain significance Osteopetrosis 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694414 SCV005193394 uncertain significance not provided criteria provided, single submitter not provided

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