ClinVar Miner

List of variants studied for Arrhythmogenic right ventricular dysplasia, familial, 14

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001792.5(CDH2):c.1306G>A (p.Asp436Asn) rs142861371 0.00009
NM_001792.5(CDH2):c.1100C>T (p.Thr367Met) rs200933425 0.00003
NM_001792.5(CDH2):c.1133A>G (p.Asn378Ser) rs199977445 0.00003
NM_001792.5(CDH2):c.14C>T (p.Ala5Val) rs1284853215 0.00003
NM_001792.5(CDH2):c.1219G>A (p.Asp407Asn) rs568089577 0.00001
NM_001792.5(CDH2):c.1604C>G (p.Thr535Ser) rs546438155 0.00001
NM_001792.5(CDH2):c.1159-1G>A rs2510799501
NM_001792.5(CDH2):c.1344+1G>A rs2143975765
NM_001792.5(CDH2):c.686A>C (p.Gln229Pro) rs965753331
NM_020317.5(RSRP1):c.520+152_520+153insC

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.