ClinVar Miner

Submissions for variant NM_014727.3(KMT2B):c.5723C>G (p.Ala1908Gly)

gnomAD frequency: 0.00034  dbSNP: rs373355746
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000896157 SCV001040236 likely benign not provided 2024-02-01 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000896157 SCV004145486 uncertain significance not provided 2024-05-01 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004551685 SCV004758764 benign KMT2B-related disorder 2020-05-26 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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.