Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs5174 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 10
rs4646 0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs775144154 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs6859 0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs8100239 0.882 0.200 19 44749847 intron variant T/A snv 0.38 5
rs2965169 0.925 0.120 19 44747899 non coding transcript exon variant A/C snv 0.50 2
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1065852 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs2234246 0.827 0.240 6 41276002 3 prime UTR variant C/T snv 0.44 5