Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs11171739 0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 4
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 2
rs2292239 0.742 0.480 12 56088396 intron variant T/G snv 0.65 2
rs10814916 0.851 0.200 9 4293150 intron variant A/C snv 0.57 2
rs3094013 1.000 0.080 6 31466589 non coding transcript exon variant G/A snv 7.6E-02 2
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 2
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 2
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 1
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 1
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 1
rs10758593 0.827 0.240 9 4292083 intron variant G/A snv 0.45 1
rs7020673 0.882 0.200 9 4291747 intron variant C/A;G snv 1