List of variants in gene NEUROD1 reported as likely benign for digestive system disorder

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

Total variants: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002500.5(NEUROD1):c.-60G>A	rs189844846	0.00441
NM_002500.5(NEUROD1):c.*719G>A	rs184299700	0.00423
NM_002500.5(NEUROD1):c.*78C>T	rs41270211	0.00315
NM_002500.4(NEUROD1):c.*1555C>T	rs192155087	0.00099
NM_002500.5(NEUROD1):c.777C>T (p.Ser259=)	rs115027760	0.00033
NM_002500.5(NEUROD1):c.738G>A (p.Pro246=)	rs115207271	0.00029
NM_002500.5(NEUROD1):c.195C>T (p.Asp65=)	rs147643871	0.00013
NM_002500.5(NEUROD1):c.1050C>G (p.Leu350=)	rs778703927	0.00006
NM_002500.5(NEUROD1):c.973C>A (p.Arg325Ser)	rs368727469	0.00004
NM_002500.5(NEUROD1):c.964G>A (p.Ala322Thr)	rs754458532	0.00003
NM_002500.5(NEUROD1):c.*1A>G
NM_002500.5(NEUROD1):c.129C>A (p.Leu43=)	rs116321775
NM_002500.5(NEUROD1):c.189T>C (p.Asp63=)	rs2105595687

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.