ClinVar Miner

Submissions for variant NM_005732.4(RAD50):c.3164+14del

dbSNP: rs148895884
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662579 SCV000785200 likely benign Nijmegen breakage syndrome-like disorder 2017-06-01 criteria provided, single submitter clinical testing
Invitae RCV002060793 SCV002405346 benign Hereditary cancer-predisposing syndrome 2024-01-26 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV000662579 SCV002538495 benign Nijmegen breakage syndrome-like disorder 2020-09-16 criteria provided, single submitter curation

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