Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs11168249 0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs17622378 0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs6651252 0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs11229555 0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs1182188 0.827 0.120 7 2830351 intron variant T/C snv 0.26 7
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs3024493 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 7
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs78534766 0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7