Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140