List of variants reported as risk factor for Obesity

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_000002.12:g.634905T>C	rs6548238	0.85166
NM_006208.3(ENPP1):c.*1043A>G	rs7754561	0.44199
NM_006208.3(ENPP1):c.517A>C (p.Lys173Gln)	rs1044498	0.32168
NM_000025.3(ADRB3):c.190T>C (p.Trp64Arg)	rs4994	0.09116
NM_016362.5(GHRL):c.269A>T (p.Gln90Leu)	rs4684677	0.06619
NM_016362.5(GHRL):c.152G>A (p.Arg51Gln)	rs34911341	0.00747
NM_004291.4(CARTPT):c.183G>C (p.Leu61Phe)	rs121909065	0.00006
NC_000012.12:g.49853685G>A	rs7138803
NM_006208.3(ENPP1):c.2101-11del	rs397832689
NM_017774.3(CDKAL1):c.371+11642G>C	rs7754840
m.15497G>A	rs199951903

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.