ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.578C>T (p.Ala193Val)

dbSNP: rs1064793928
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001183850 SCV001349692 uncertain significance Hereditary cancer-predisposing syndrome 2019-01-31 criteria provided, single submitter clinical testing
Baylor Genetics RCV003469302 SCV004210206 uncertain significance Familial cancer of breast 2023-07-03 criteria provided, single submitter clinical testing

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