ClinVar Miner

Submissions for variant NM_003839.4(TNFRSF11A):c.*321del

dbSNP: rs886054088
Minimum review status: Collection method:
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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 RCV000398720 SCV000410047 uncertain significance Osteopetrosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000297001 SCV000410048 uncertain significance Bone Paget disease 2016-06-14 criteria provided, single submitter clinical testing

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