Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs79105258 12 111280427 intron variant C/A;T snv 24
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1004467 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs1859168 0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 13
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs3918226 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs11014166 0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs11191548 0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492 0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs633185 0.925 0.080 11 100722807 intron variant G/A;C snv 10