ClinVar Miner

Submissions for variant NM_005732.4(RAD50):c.495T>C (p.Pro165=)

dbSNP: rs1554097778
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000548927 SCV000628302 likely benign Hereditary cancer-predisposing syndrome 2019-03-26 criteria provided, single submitter clinical testing

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