ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.2898C>A (p.Thr966=)

dbSNP: rs772786755
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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 RCV001179022 SCV001343592 likely benign Hereditary cancer-predisposing syndrome 2020-02-09 criteria provided, single submitter clinical testing
Invitae RCV002558897 SCV003327819 likely benign Hereditary nonpolyposis colorectal neoplasms 2022-03-11 criteria provided, single submitter clinical testing

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