ClinVar Miner

Submissions for variant NM_005732.4(RAD50):c.2274T>C (p.Asn758=)

dbSNP: rs2149846916
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001437535 SCV001640389 likely benign Hereditary cancer-predisposing syndrome 2020-09-24 criteria provided, single submitter clinical testing

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