ClinVar Miner

Submissions for variant NM_005502.4(ABCA1):c.2115+17C>T

gnomAD frequency: 0.00054  dbSNP: rs371944946
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 RCV002119035 SCV002446963 likely benign not provided 2025-01-22 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003331317 SCV004038413 uncertain significance not specified 2023-08-01 criteria provided, single submitter clinical testing

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