List of variants reported as likely benign for Arrhythmogenic right ventricular dysplasia 12

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002230.4(JUP):c.425G>A (p.Arg142His)	rs41283425	0.03910
NM_002230.4(JUP):c.*709G>C	rs56339743	0.03348
NM_002230.4(JUP):c.*286C>T	rs73983656	0.03337
NM_002230.4(JUP):c.*853C>T	rs55919561	0.01530
NM_002230.4(JUP):c.*623G>A	rs55634776	0.01451
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.1563A>G (p.Ala521=)	rs149926974	0.00753
NM_002230.4(JUP):c.*1027G>C	rs147905567	0.00640
NM_002230.4(JUP):c.*2C>T	rs112879398	0.00630
NM_002230.4(JUP):c.1224C>T (p.Leu408=)	rs2230408	0.00620
NM_002230.4(JUP):c.1774-13C>T	rs116772523	0.00553
NM_002230.4(JUP):c.*239G>A	rs115919416	0.00526
NM_002230.4(JUP):c.777C>T (p.Gly259=)	rs34890640	0.00507
NM_002230.4(JUP):c.1959C>T (p.Ser653=)	rs375451560	0.00012
NM_002230.4(JUP):c.1774-6C>T	rs375016135	0.00007

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.