Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs63750743
rs63750743
0.925 0.080 3 14141665 missense variant C/T snv
Arrhythmogenic Right Ventricular Dysplasia
0.770 1.000 6 2008 2019
dbSNP: rs63750743
rs63750743
0.925 0.080 3 14141665 missense variant C/T snv
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder)
0.800 1.000 4 2008 2017