Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1271572 0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs3087456 0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs3730358 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs4704397 0.807 0.200 5 77222617 intron variant G/A snv 0.54 13
rs6742078 0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs10846744 0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs12041331 0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs10507391 0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs1343151 0.752 0.400 1 67253446 intron variant G/A snv 0.41 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs6903956 0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs7069102 0.790 0.440 10 67903362 intron variant C/G snv 0.64 10