Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34608001 0.827 0.080 16 1079441 synonymous variant G/A snv 1.7E-02 1.5E-02 5
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2839350 0.827 0.080 21 46597307 downstream gene variant G/A snv 0.22 5
rs3788266 0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs2076137 0.807 0.080 22 50077337 intron variant C/T snv 0.14 6
rs2235349 0.807 0.080 22 50079810 intron variant T/C snv 0.22 6
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42