Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10776934 1.000 0.080 9 135137855 regulatory region variant T/G snv 0.74 1
rs11966728 1.000 0.080 6 131955465 intron variant T/C snv 0.26 1
rs12972991 1.000 0.080 19 39241107 upstream gene variant A/C snv 0.19 1
rs12980602 1.000 0.080 19 39262180 upstream gene variant T/C snv 0.25 1
rs4803223 1.000 0.080 19 39255579 upstream gene variant A/G snv 0.13 1
rs8109886 1.000 0.080 19 39252122 upstream gene variant C/A snv 0.53 1
rs965469 1.000 0.080 20 3400902 intron variant T/C snv 0.20 1
rs11697186 1.000 0.080 20 3204477 intron variant A/C;T snv 7.0E-02 1
rs10789491 1.000 0.080 1 46713638 intron variant A/G snv 0.80 1
rs28416813 1.000 0.080 19 39245004 5 prime UTR variant C/G snv 0.31 0.39 1
rs6139030 1.000 0.080 20 3207087 upstream gene variant T/C snv 8.6E-02 1
rs12952093 1.000 0.080 17 78367559 intron variant A/C;T snv 1
rs1293762 1.000 0.080 12 112993031 intron variant T/G snv 0.67 1
rs2779180 1.000 0.080 19 4841139 intron variant A/G snv 0.37 1
rs1470452230 0.925 0.120 9 135561895 missense variant A/C snv 7.0E-06 2
rs12989760 0.925 0.120 2 250470 intron variant T/C snv 2
rs11854484 0.925 0.120 15 45253280 missense variant C/T snv 0.47 0.45 2
rs6051702 0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs2230201
C3
0.882 0.200 19 6713280 synonymous variant C/G;T snv 0.19 3
rs1863918 0.882 0.160 5 179112381 3 prime UTR variant G/T snv 0.25 4
rs2267716 0.851 0.120 7 30677027 intron variant T/A;C snv 4
rs9695310 0.851 0.120 9 32464137 intron variant G/C snv 0.52 4
rs11506105 0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs4803217 0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs8103142 0.882 0.120 19 39244466 missense variant T/C snv 0.29 0.40 4