List of variants reported as benign for Arrhythmogenic right ventricular dysplasia 5 by All of Us Research Program, National Institutes of Health

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024334.3(TMEM43):c.536T>C (p.Met179Thr)	rs2340917	0.35127
NM_024334.3(TMEM43):c.504A>T (p.Lys168Asn)	rs4685076	0.29043
NM_024334.3(TMEM43):c.163-14C>T	rs113745859	0.02553
NM_024334.3(TMEM43):c.909C>T (p.Ser303=)	rs35100587	0.02012
NM_024334.3(TMEM43):c.222C>T (p.Pro74=)	rs34099410	0.00841
NM_024334.3(TMEM43):c.82C>T (p.Arg28Trp)	rs35028636	0.00535
NM_024334.3(TMEM43):c.163-6T>A	rs372434224	0.00088
NM_024334.3(TMEM43):c.45C>A (p.Val15=)	rs150334659	0.00041
NM_024334.3(TMEM43):c.921G>A (p.Lys307=)	rs201771608	0.00006
NM_024334.3(TMEM43):c.246G>A (p.Pro82=)	rs376098518	0.00001

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.