Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1126407 0.925 0.200 1 236537507 missense variant T/A snv 0.61 0.61 3
rs11264799 0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1310182 0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2488457 0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs33996649 0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs3761959 0.827 0.320 1 157699488 intron variant C/A;G;T snv 7
rs3789604 0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs3890745 0.925 0.200 1 2622185 intron variant T/C snv 0.40 4
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs864537 0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs945635 0.882 0.200 1 157700500 5 prime UTR variant C/A;G snv 5.6E-05; 0.45 4
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9