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
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs7632505 0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179 0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16