ClinVar Miner

Submissions for variant NM_001366385.1(CARD14):c.-8G>T

dbSNP: rs367878757
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002264596 SCV002543340 benign Autoinflammatory syndrome 2019-05-01 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003926350 SCV004743499 benign CARD14-related disorder 2019-05-22 criteria provided, single submitter 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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