List of variants in gene PTF1A reported as benign for diabetes mellitus

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_178161.3(PTF1A):c.787T>C (p.Ser263Pro)	rs7918487	0.51842
NC_000010.11:g.23177805G>A	rs7916519	0.48352
NC_000010.11:g.23163713A>G	rs10741021	0.23437
NC_000010.11:g.23189850T>G	rs4748844	0.08608
NM_178161.3(PTF1A):c.*15G>A	rs10828415	0.08608
NM_178161.3(PTF1A):c.269G>C (p.Gly90Ala)	rs535090775	0.00423
NC_000010.11:g.23167584A>C	rs16923098	0.00379
NM_178161.3(PTF1A):c.386C>T (p.Ala129Val)	rs370163562	0.00109
NC_000010.11:g.23187502G>A	rs187391034	0.00038

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.