ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.7437A>G (p.Glu2479=)

dbSNP: rs1591160964
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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 RCV001479218 SCV001683511 likely benign Ataxia-telangiectasia syndrome 2023-01-23 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004588427 SCV005081905 benign Familial cancer of breast 2024-06-14 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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