List of variants in gene JUP reported as benign by PreventionGenetics, part of Exact Sciences

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_002230.4(JUP):c.909+17T>C	rs12942034	0.81403
NM_002230.4(JUP):c.213T>C (p.Asp71=)	rs7405731	0.77675
NM_002230.4(JUP):c.2046+22A>G	rs7216034	0.77249
NM_002230.4(JUP):c.1774-34C>A	rs8067890	0.71145
NM_002230.4(JUP):c.2089A>T (p.Met697Leu)	rs1126821	0.66611
NM_002230.4(JUP):c.909+49T>C	rs77529236	0.05038
NM_002230.4(JUP):c.1653+10C>A	rs73983658	0.04634
NM_002230.4(JUP):c.469-48C>T	rs75715269	0.03700
NM_002230.4(JUP):c.405C>T (p.Asp135=)	rs17850807	0.03356
NM_002230.4(JUP):c.2047-14C>G	rs116666639	0.00819
NM_002230.4(JUP):c.1942G>A (p.Val648Ile)	rs143043662	0.00760
NM_002230.4(JUP):c.1774-13C>T	rs116772523	0.00553
NM_002230.4(JUP):c.777C>T (p.Gly259=)	rs34890640	0.00507

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.