ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.8585-6C>T

dbSNP: rs2137077591
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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 RCV002200020 SCV002359126 likely benign Ataxia-telangiectasia syndrome 2024-01-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004591746 SCV005085633 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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