ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3557-10T>G

dbSNP: rs2104521319
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Sema4, Sema4 RCV002255869 SCV002528041 likely benign Hereditary cancer-predisposing syndrome 2020-11-28 criteria provided, single submitter curation
Labcorp Genetics (formerly Invitae), Labcorp RCV003101409 SCV003507067 likely benign Hereditary nonpolyposis colorectal neoplasms 2022-05-31 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV002255869 SCV004357733 uncertain significance Hereditary cancer-predisposing syndrome 2023-06-14 criteria provided, single submitter clinical testing This variant causes a T to G nucleotide substitution at the -10 position of intron 6 of the MSH6 gene. To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with MSH6-related disorders in the literature. This variant has not been identified in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.