Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs3741378 0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 8
rs6795735 0.882 0.120 3 64719689 intron variant C/A;G;T snv 7
rs2067087 1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs1250259 1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs4823006 22 29055683 3 prime UTR variant A/G snv 0.41 5
rs936226 15 74776941 intergenic variant C/T snv 0.69 3