Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 3
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs9282858 0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 7
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 3
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 3
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 5
rs10514299 0.827 0.120 5 88367793 intron variant C/T snv 0.21 1
rs1039002 0.851 0.080 6 165741969 intron variant G/A;T snv 1
rs10392 0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 6
rs139438618 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4
rs2066702 0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 3
rs12912251 0.882 0.080 15 38694167 intron variant G/T snv 0.25 2
rs12898460 0.882 0.080 15 38694612 intron variant C/T snv 0.23 1
rs6943555 0.882 0.080 7 70341037 intron variant T/A snv 0.34 1