ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.847-6T>G

dbSNP: rs1555917050
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000663238 SCV000786442 uncertain significance Familial cancer of breast 2018-05-02 criteria provided, single submitter clinical testing
Invitae RCV000663238 SCV001670266 likely benign Familial cancer of breast 2018-02-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000663238 SCV004020074 uncertain significance Familial cancer of breast 2023-03-07 criteria provided, single submitter clinical testing This variant is classified as a variant of uncertain significance as there is insufficient evidence to determine its impact on protein function and/or cancer risk.

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