Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1033656351 0.827 0.160 12 121232997 missense variant G/A snv 1.6E-05 2.8E-05 7
rs1718119 0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249