Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11168249 0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11229555 0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs11230563 0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 8
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs11614178 0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs1182188 0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs11938228 0.882 0.120 4 153700794 intron variant C/A;T snv 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1250546 0.925 0.080 10 79272775 intron variant A/G snv 0.36 3
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12718244 0.827 0.120 7 50136058 intron variant G/A snv 0.33 0.33 6
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs12942547 0.807 0.200 17 42375526 intron variant A/G;T snv 7
rs13407913 0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 7
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs17622378 0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs17780256 0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6