ClinVar Miner

Submissions for variant NM_004048.4(B2M):c.279T>C (p.Thr93=)

gnomAD frequency: 0.00005  dbSNP: rs766309912
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 RCV001448619 SCV001651715 likely benign Hypoproteinemia, hypercatabolic 2022-07-12 criteria provided, single submitter clinical testing

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