ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.3284+8dup

dbSNP: rs886047611
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000374329 SCV000367043 uncertain significance Ataxia-telangiectasia syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000374329 SCV001616318 likely benign Ataxia-telangiectasia syndrome 2025-02-03 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004591116 SCV005082782 likely benign Familial cancer of breast 2024-05-14 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.
Department of Pathology and Laboratory Medicine, Sinai Health System RCV004591116 SCV005919072 uncertain significance Familial cancer of breast 2019-10-02 criteria provided, single submitter clinical testing

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