ClinVar Miner

Submissions for variant NM_001048166.1(STIL):c.873-6G>T

dbSNP: rs375670720
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000180589 SCV000233060 uncertain significance not provided 2015-02-23 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003967446 SCV004776612 likely benign STIL-related disorder 2020-01-09 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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