ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.8584+7T>G

dbSNP: rs1374271708
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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 RCV000542737 SCV000622834 likely benign Ataxia-telangiectasia syndrome 2022-06-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004592539 SCV005082067 likely benign Familial cancer of breast 2024-06-20 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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