Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs2395029 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs7439366 0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs765502022 0.827 0.240 4 69112695 missense variant T/C snv 1.6E-05 8
rs28399499 0.827 0.280 19 41012316 missense variant T/C snv 5.1E-03 2.2E-02 6
rs1188975135 0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 4
rs1292288729 1.000 19 41009375 missense variant T/C snv 7.4E-06 1
rs774027752 1.000 19 40845472 missense variant T/C snv 8.0E-06 1.4E-05 1
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs57302492 1.000 2 70831099 missense variant T/A snv 7.0E-02 8.9E-02 1
rs756151230 1.000 7 92470377 missense variant G/C snv 1
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs14158 0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs7248668 0.925 0.080 19 39253181 upstream gene variant G/A snv 0.16 3
rs1272938495 1.000 2 136115225 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1433591886 1.000 2 169633213 missense variant G/A snv 4.0E-06 1
rs3740996 1.000 11 5680051 missense variant G/A snv 0.13 0.10 1