ClinVar Miner

Submissions for variant NM_003839.4(TNFRSF11A):c.327C>T (p.Pro109=)

gnomAD frequency: 0.00491  dbSNP: rs35003467
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000178199 SCV000230216 benign not specified 2015-02-11 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000178199 SCV000309843 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000954312 SCV001100937 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000954312 SCV004143223 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing TNFRSF11A: BP4, BP7, BS2
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000954312 SCV001927417 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000954312 SCV001974093 likely benign not provided no assertion criteria provided clinical testing

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