rs41272699, DES

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Myofibrillar Myopathy
CUI: C2678065
Disease: Myofibrillar Myopathy
24 0.925 0.160 2 219420154 missense variant C/T snv 9.2E-03 1.0E-02 0.700 0
Arrhythmogenic Right Ventricular Dysplasia
CUI: C0349788
Disease: Arrhythmogenic Right Ventricular Dysplasia
136 0.925 0.160 2 219420154 missense variant C/T snv 9.2E-03 1.0E-02 0.010 1 2013 2013