Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6016142 1.000 0.120 20 39672165 intergenic variant C/T snv 7.8E-02 3
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 3
rs7838717
BOP1
1.000 0.120 8 144280310 intron variant C/T snv 0.30 3
rs38904 1.000 0.120 7 117252792 intergenic variant T/C snv 0.52 2
rs9525927 0.925 0.160 13 44268367 regulatory region variant G/A snv 0.80 2
rs2598107
SFRP4 ; EPDR1
1.000 0.120 7 37933412 intron variant C/T snv 0.34 2
rs10809650 0.925 0.120 9 1202371 intergenic variant A/G snv 0.26 1
rs12342106 1.000 0.120 9 1201156 regulatory region variant G/A snv 0.32 1
rs2179367 0.925 0.120 6 149441401 regulatory region variant A/G snv 0.50 1
rs4932194 0.925 0.120 15 88702008 regulatory region variant A/C;G;T snv 1
rs6102095 1.000 0.120 20 40692111 upstream gene variant G/A;C snv 1
rs6496519 1.000 0.120 15 88694953 intergenic variant C/T snv 0.16 1
rs6519955 0.925 0.120 22 46025962 regulatory region variant G/T snv 0.50 1
rs7071275 1.000 0.120 10 121662920 regulatory region variant C/T snv 0.19 1
rs8124695 0.925 0.120 20 40399796 intergenic variant C/A;T snv 1
rs1032466
ATL1
1.000 0.120 14 50607743 intron variant A/C snv 0.27 1
rs4789939
CEP295NL ; TIMP2
0.925 0.120 17 78885621 intron variant T/A;C snv 1
rs977987
CHST6
1.000 0.120 16 75472695 3 prime UTR variant G/A snv 0.52 1
rs17433710
DDR2
1.000 0.120 1 162702221 intron variant T/C snv 0.12 1
rs11672517
DUXA
0.925 0.120 19 57166826 intron variant G/A snv 0.24 1
rs10866846
EBF2
1.000 0.120 8 25988159 intron variant G/A snv 0.32 1
rs611744
EIF3E
0.925 0.120 8 108215779 intron variant A/G;T snv 1
rs16879765
EPDR1 ; SFRP4
0.925 0.120 7 37949493 intron variant C/T snv 0.13 1
rs2306022
ITGA11
0.851 0.160 15 68335825 missense variant C/T snv 6.6E-02 5.8E-02 1
rs2912522
LINC01592
0.925 0.120 8 69080145 intron variant G/A snv 0.73 1