Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs79105258 12 111280427 intron variant C/A;T snv 23
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 20
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
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
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17