ClinVar Miner

Submissions for variant NM_004048.4(B2M):c.168A>G (p.Glu56=)

gnomAD frequency: 0.00001  dbSNP: rs1347307081
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001405136 SCV001607053 likely benign Hypoproteinemia, hypercatabolic 2022-01-13 criteria provided, single submitter clinical testing

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