ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.1236-3dup (rs34325032)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000159602 SCV000183861 benign Hereditary cancer-predisposing syndrome 2013-10-11 criteria provided, single submitter clinical testing
Color RCV000159602 SCV000687292 likely benign Hereditary cancer-predisposing syndrome 2017-06-29 criteria provided, single submitter clinical testing
GeneDx RCV000159602 SCV000209586 benign Hereditary cancer-predisposing syndrome 2014-02-18 criteria provided, single submitter clinical testing The variant is found in PANC-HEREDIC,BR-OV-HEREDIC panel(s).

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