ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.137A>G (p.His46Arg)

dbSNP: rs1591447177
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799187 SCV002042456 uncertain significance Breast and/or ovarian cancer 2019-09-25 criteria provided, single submitter clinical testing

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