Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33