ClinVar Miner

Submissions for variant NM_006509.4(RELB):c.496G>A (p.Ala166Thr)

gnomAD frequency: 0.00014  dbSNP: rs200472617
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002197398 SCV002359137 likely benign not provided 2024-12-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002197398 SCV005208551 likely benign not provided criteria provided, single submitter not provided

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