ClinVar Miner

Submissions for variant NM_003839.4(TNFRSF11A):c.1296G>A (p.Pro432=)

gnomAD frequency: 0.00006  dbSNP: rs547088539
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
Eurofins Ntd Llc (ga) RCV000392841 SCV000338398 uncertain significance not provided 2016-01-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000392841 SCV001065389 likely benign not provided 2025-01-31 criteria provided, single submitter clinical testing

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