ClinVar Miner

Submissions for variant NM_005732.4(RAD50):c.2525-6G>A

dbSNP: rs745693687
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000861059 SCV001001270 likely benign Hereditary cancer-predisposing syndrome 2023-11-17 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003975366 SCV004799001 likely benign RAD50-related condition 2021-11-17 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).

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