ClinVar Miner

Submissions for variant NM_006509.4(RELB):c.948C>T (p.Thr316=)

gnomAD frequency: 0.00004  dbSNP: rs368859963
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002107762 SCV002399891 likely benign not provided 2024-07-16 criteria provided, single submitter clinical testing

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