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
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
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
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
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
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23