ClinVar Miner

Submissions for variant NM_005502.4(ABCA1):c.5636+18A>C

gnomAD frequency: 0.00056  dbSNP: rs111671370
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 RCV002156035 SCV002470720 benign not provided 2023-12-02 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003324000 SCV004028925 uncertain significance not specified 2023-07-18 criteria provided, single submitter clinical testing

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