ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.-371G>C

gnomAD frequency: 0.00019  dbSNP: rs890835455
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000499990 SCV000593492 uncertain significance not specified 2016-10-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002476003 SCV002779730 uncertain significance Familial cancer of breast; Ataxia-telangiectasia syndrome 2021-11-18 criteria provided, single submitter clinical testing

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