Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs7120118 0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16