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
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs12273363 0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs17070145 0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs356219 0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs3764650 0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs10748842 0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs157582 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 8
rs17518584 0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs363050 0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs10524523 0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 7
rs140701 0.790 0.200 17 30211514 intron variant C/T snv 0.40 7
rs2251214 0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs1018381 0.882 0.040 6 15656839 intron variant G/A snv 0.16 6