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
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
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
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
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
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
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
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
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1271572 0.708 0.400 14 64295199 intron variant A/C;T snv 16