ClinVar Miner

Submissions for variant NM_001643.2(APOA2):c.53-43TG[16]

dbSNP: rs17244502
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000394607 SCV000350152 uncertain significance Apolipoprotein A-II deficiency 2016-06-14 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001194249 SCV001363637 benign not specified 2019-08-12 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003967824 SCV004793783 benign APOA2-related disorder 2024-01-28 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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