Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs12914385 0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 7
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs2710323 0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 6
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs2252865 0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs9371601 0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 6
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5