ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.8269-9T>C

dbSNP: rs2136938827
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001399871 SCV001601671 likely benign Ataxia-telangiectasia syndrome 2023-11-30 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004590389 SCV005085624 likely benign Familial cancer of breast 2024-06-19 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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