ClinVar Miner

Submissions for variant NM_003839.4(TNFRSF11A):c.-39G>A

gnomAD frequency: 0.28496  dbSNP: rs7238731
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000249802 SCV000309840 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000312036 SCV000409991 likely benign Osteopetrosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000370833 SCV000409992 likely benign Bone Paget disease 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001683040 SCV001905077 benign not provided 2021-06-19 criteria provided, single submitter clinical testing

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