ClinVar Miner

Submissions for variant NM_000071.3(CBS):c.829-8C>G

dbSNP: rs750081937
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002235913 SCV001013274 likely benign HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED 2023-05-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV000871596 SCV001455976 uncertain significance Classic homocystinuria 2020-01-24 no assertion criteria provided clinical testing

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