ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3138C>T (p.Asp1046=)

dbSNP: rs1244049824
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000556064 SCV000624819 likely benign Hereditary nonpolyposis colorectal neoplasms 2017-01-19 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257783 SCV002535793 likely benign Hereditary cancer-predisposing syndrome 2021-09-02 criteria provided, single submitter curation

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