ClinVar Miner

Submissions for variant NM_004048.4(B2M):c.147G>T (p.Gly49=)

dbSNP: rs768464174
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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 RCV002130536 SCV002444014 likely benign Hypoproteinemia, hypercatabolic 2023-10-03 criteria provided, single submitter clinical testing

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