ClinVar Miner

Submissions for variant NM_007194.4(CHEK2):c.908+18T>A (rs755416802)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000582934 SCV000689744 likely benign Hereditary cancer-predisposing syndrome 2016-10-24 criteria provided, single submitter clinical testing
Counsyl RCV000662851 SCV000785718 likely benign Familial cancer of breast 2017-11-08 criteria provided, single submitter clinical testing

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