ClinVar Miner

Submissions for variant NM_018662.3(DISC1):c.2295T>A (p.Gly765=)

gnomAD frequency: 0.00013  dbSNP: rs367543098
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV003964954 SCV004780418 likely benign DISC1-related condition 2021-06-17 criteria provided, single submitter 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).
Psychiatry Genetics Yale University RCV000084651 SCV000116787 not provided not provided no assertion provided not provided

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