ClinVar Miner

Submissions for variant NM_003839.4(TNFRSF11A):c.1515G>A (p.Ala505=)

gnomAD frequency: 0.00004  dbSNP: rs374310569
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) RCV000728875 SCV000856493 uncertain significance not provided 2017-09-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000728875 SCV002449212 likely benign not provided 2024-12-20 criteria provided, single submitter clinical testing

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