Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs12914385 0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs886424 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs3131296 0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs9272535 0.827 0.280 6 32638979 synonymous variant G/A snv 3.0E-05 1.8E-03 5
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs8283 0.882 0.120 6 32115523 3 prime UTR variant A/G snv 0.25 4
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs8042374 0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs389883 0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 4
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 4