ClinVar Miner

Submissions for variant NM_015506.3(MMACHC):c.430-10C>T

dbSNP: rs550692873
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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 RCV002078135 SCV002321463 likely benign Cobalamin C disease 2021-08-13 criteria provided, single submitter clinical testing

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