ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.901+6A>C

dbSNP: rs1555067357
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000544763 SCV000622877 likely benign Ataxia-telangiectasia syndrome 2023-11-15 criteria provided, single submitter clinical testing
Counsyl RCV000544763 SCV000799550 uncertain significance Ataxia-telangiectasia syndrome 2018-04-25 criteria provided, single submitter clinical testing

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