ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.8094A>G (p.Leu2698=) (rs786203569)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000166947 SCV000217767 likely benign Hereditary cancer-predisposing syndrome 2014-11-24 criteria provided, single submitter clinical testing
Color RCV000166947 SCV000904743 likely benign Hereditary cancer-predisposing syndrome 2018-09-04 criteria provided, single submitter clinical testing
Invitae RCV000952587 SCV001099102 likely benign Ataxia-telangiectasia syndrome 2019-12-31 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV001174986 SCV001338476 likely benign not specified 2020-04-17 criteria provided, single submitter clinical testing

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