ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.5310A>G (p.Ser1770=) (rs1060504282)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000476371 SCV000558345 likely benign Ataxia-telangiectasia syndrome 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000561273 SCV000667871 likely benign Hereditary cancer-predisposing syndrome 2016-01-17 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Color RCV000561273 SCV000910424 likely benign Hereditary cancer-predisposing syndrome 2018-07-03 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV001193038 SCV001361583 likely benign not specified 2019-07-18 criteria provided, single submitter clinical testing

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