List of variants reported as 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: 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.*225T>C	rs4627408	0.70932
NM_002230.4(JUP):c.2089A>T (p.Met697Leu)	rs1126821	0.66611
NM_002230.4(JUP):c.-88A>G	rs4796702	0.65910
NM_002230.4(JUP):c.1653+10C>A	rs73983658	0.04634
NM_002230.4(JUP):c.425G>A (p.Arg142His)	rs41283425	0.03910
NM_002230.4(JUP):c.405C>T (p.Asp135=)	rs17850807	0.03356
NM_002230.4(JUP):c.*669C>T	rs8074883	0.01622
NM_002230.4(JUP):c.867C>T (p.Thr289=)	rs2230407	0.01591
NM_002230.4(JUP):c.1159-13C>A	rs201627219	0.00258

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.