Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 42
rs3184504 0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67 31
rs964184 0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83 31
rs780094 0.699 0.286 2 27518370 intron variant T/C snp 0.67 29
rs4420638 0.724 0.321 19 44919689 intergenic variant A/G snp 0.19 25
rs2476601 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 22
rs10401969 0.801 0.214 19 19296909 intron variant T/C snp 9.8E-02 20
rs653178 0.692 0.429 12 111569952 intron variant C/T snp 0.67 19
rs174547 0.846 0.071 11 61803311 intron variant T/C snp 0.30 18
rs6679677 0.679 0.250 1 113761186 intergenic variant C/A snp 8.2E-02 18
rs247617 0.846 0.107 16 56956804 regulatory region variant C/A snp 0.29 17
rs1333049 0.715 0.286 9 22125504 intergenic variant G/C snp 0.41 17
rs629301 0.878 0.071 1 109275684 3 prime UTR variant G/T snp 0.75 17
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 17
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 17
rs4506565 0.821 0.143 10 112996282 intron variant A/G,T snp 6.4E-05; 0.32 17
rs562338 0.846 0.143 2 21065449 intergenic variant A/G snp 0.71 16
rs1728918 0.846 0.107 2 27412596 intergenic variant A/G,T snp 0.79 16
rs7703051 0.878 0.071 5 75329662 intron variant C/A snp 0.39 16
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 16
rs671 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 16
rs12579302 0.878 0.071 12 89656726 intron variant A/G snp 0.14 16
rs4803750 0.821 0.214 19 44744370 intergenic variant A/G snp 7.3E-02 16
rs261332 0.878 0.071 15 58435126 non coding transcript exon variant A/G snp 0.79 16
rs799165 0.878 0.071 7 73637727 intergenic variant T/A snp 0.13 15