Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10010131 0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10146997 0.827 0.240 14 79478819 intron variant A/G snv 0.25 6
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10423928 0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs1044250 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1058046
PYY
0.925 0.120 17 43953163 missense variant G/C snv 0.63 0.59 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10885406 0.925 0.120 10 113017965 intron variant A/G snv 0.55 2
rs10895068 0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs10946398 0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs10968576 0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs11075989
FTO
0.925 0.120 16 53785965 intron variant C/A;T snv 3
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6