Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7582472 2 133887223 regulatory region variant T/C snv 0.21 1
rs755001634 0.763 0.280 11 49154384 stop gained G/A snv 1.2E-05 13
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs2229094 0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 17
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs368939818 0.763 0.280 11 49156734 missense variant G/A snv 4.0E-05 2.1E-05 13
rs1200746244 0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs1409851868 0.882 0.080 3 89399325 missense variant A/G snv 6
rs77960347 18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 6
rs115482041 0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 4
rs757891309
MTR
0.882 0.120 1 236850389 missense variant C/A;T snv 4.0E-06; 4.0E-06 4