ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.3747-10C>G (rs775274473)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000583321 SCV000687497 likely benign Hereditary cancer-predisposing syndrome 2017-07-28 criteria provided, single submitter clinical testing
Counsyl RCV000227510 SCV000799518 uncertain significance Ataxia-telangiectasia syndrome 2018-04-24 criteria provided, single submitter clinical testing
Invitae RCV000227510 SCV000282941 likely benign Ataxia-telangiectasia syndrome 2017-07-24 criteria provided, single submitter clinical testing

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