ClinVar Miner

Submissions for variant NM_019844.4(SLCO1B3):c.728-4C>G

dbSNP: rs759435706
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001023 SCV001158131 uncertain significance not specified 2019-02-06 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003983817 SCV004797192 likely benign SLCO1B3-related disorder 2023-12-15 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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