List of variants reported as likely benign for Maturity-onset diabetes of the young type 11 by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001715.3(BLK):c.211G>A (p.Ala71Thr)	rs55758736	0.01485
NM_001715.3(BLK):c.102C>T (p.Asp34=)	rs75383960	0.00743
NM_001715.3(BLK):c.1338C>G (p.Arg446=)	rs377160616	0.00073
NM_001715.3(BLK):c.1075C>T (p.Arg359Cys)	rs146505280	0.00059
NM_001715.3(BLK):c.368+13G>A	rs199644751	0.00024
NM_001715.3(BLK):c.424A>G (p.Ile142Val)	rs562247916	0.00021
NM_001715.3(BLK):c.772+16C>T	rs200129390	0.00011
NM_001715.3(BLK):c.859G>A (p.Val287Met)	rs1042687	0.00007
NM_001715.3(BLK):c.675G>A (p.Pro225=)	rs761122806	0.00006
NM_001715.3(BLK):c.465C>G (p.Thr155=)	rs375035401	0.00004
NM_001715.3(BLK):c.27G>A (p.Pro9=)	rs536630306	0.00002
NM_001715.3(BLK):c.1371C>T (p.Pro457=)	rs1356289485	0.00001
NM_001715.3(BLK):c.269+13G>C	rs144839649
NM_001715.3(BLK):c.591G>T (p.Ser197=)	rs140834602

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.