ClinVar Miner

Submissions for variant NM_001130823.3(DNMT1):c.3939C>T (p.Gly1313=) (rs142903301)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000243364 SCV000306770 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000296832 SCV000410217 likely benign Dementia, Deafness, and Sensory Neuropathy 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000544232 SCV000651305 benign Hereditary sensory neuropathy type IE 2017-08-08 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000991908 SCV001143762 benign not provided 2018-11-20 criteria provided, single submitter clinical testing

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.