ClinVar Miner

Submissions for variant NM_014324.6(AMACR):c.553-14C>T

dbSNP: rs767051900
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002182699 SCV002342930 likely benign Alpha-methylacyl-CoA racemase deficiency 2022-06-13 criteria provided, single submitter clinical testing

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