Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs766914563 0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs3921 0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs10336 0.851 0.240 4 76001835 3 prime UTR variant A/G;T snv 4
rs10892151 1.000 11 117661016 intron variant C/T snv 9.7E-02 3
rs11881222 0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs4619915 0.882 0.120 4 76034048 3 prime UTR variant A/G snv 0.61 3
rs7248668 0.925 0.080 19 39253181 upstream gene variant G/A snv 0.16 3
rs1194919682 0.925 0.040 2 136115158 missense variant A/G snv 2
rs1292288729 1.000 19 41009375 missense variant T/C snv 7.4E-06 1
rs4657412 1.000 1 165207796 intron variant G/A snv 0.79 1
rs756151230 1.000 7 92470377 missense variant G/C snv 1
rs371074389 0.732 0.320 2 136115226 synonymous variant C/T snv 4.0E-06 4.2E-05 16
rs1272938495 1.000 2 136115225 missense variant G/A snv 4.0E-06 7.0E-06 1
rs781172058 0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs749569169 1.000 7 29512676 missense variant A/G snv 4.0E-06 1
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30