ClinVar Miner

Submissions for variant NM_004048.4(B2M):c.126C>T (p.Phe42=)

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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 RCV003517612 SCV004325448 likely benign Hypoproteinemia, hypercatabolic 2023-10-04 criteria provided, single submitter clinical testing

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