ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.7038A>G (p.Ala2346=)

dbSNP: rs146167034
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000590767 SCV000694343 likely benign not specified 2019-08-21 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000772499 SCV000905678 likely benign Hereditary cancer-predisposing syndrome 2018-07-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001471256 SCV001675360 likely benign Ataxia-telangiectasia syndrome 2023-11-21 criteria provided, single submitter clinical testing

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