ClinVar Miner

Submissions for variant NM_004048.4(B2M):c.68-12G>A

gnomAD frequency: 0.00003  dbSNP: rs375970981
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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 RCV002168191 SCV002341212 likely benign Hypoproteinemia, hypercatabolic 2023-12-13 criteria provided, single submitter clinical testing

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