Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs144995469 1.000 0.080 14 56732364 upstream gene variant C/T snv 8.6E-03 1
rs2445284 1.000 0.080 11 5008473 downstream gene variant C/T snv 0.57 1
rs3115229 1.000 0.080 4 122088578 upstream gene variant T/C snv 9.9E-03 1
rs543023132 1.000 0.080 6 155652652 downstream gene variant TTTTT/-;T;TT;TTT;TTTT;TTTTTT;TTTTTTT delins 0.12 1
rs33930165
HBB
0.882 0.120 11 5227003 missense variant C/G;T snv 9.2E-04; 4.4E-05 1
rs7948471
HBE1 ; HBG2 ; OR51B5 ; OR51I2
1.000 0.080 11 5450516 intron variant G/A snv 0.47 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs9714060
MUC4
1.000 0.080 3 195760605 intron variant A/C;G snv 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs146893001
PTPN3
1.000 0.080 9 109419337 intron variant T/C snv 3.9E-03 1
rs7216169
RABEP1
1.000 0.080 17 5316216 intron variant C/T snv 0.12 1
rs4234795
SORCS2
1.000 0.080 4 7209075 intron variant A/C;G;T snv 1
rs11968814 1.000 0.080 6 71067268 intergenic variant G/A snv 4.4E-02 2
rs1669539 1.000 0.080 2 105998818 intergenic variant T/C snv 7.1E-02 2
rs7952106 1.000 0.080 11 113553836 regulatory region variant G/T snv 0.71 2
rs67072384
ARAP1
0.925 0.080 11 72739679 intron variant C/T snv 0.14 2
rs10172646
BCL11A
1.000 0.080 2 60493622 intron variant G/A snv 0.64 2
rs10195871
BCL11A
1.000 0.080 2 60493454 intron variant A/G;T snv 2
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 2
rs1427407
BCL11A
0.827 0.120 2 60490908 intron variant T/C;G snv 2
rs1896294
BCL11A
1.000 0.080 2 60491939 intron variant C/G;T snv 2
rs1896295
BCL11A
1.000 0.080 2 60496951 intron variant T/C snv 0.81 2
rs1896296
BCL11A
1.000 0.080 2 60496952 intron variant G/T snv 0.80 2
rs6545816
BCL11A
1.000 0.080 2 60487726 intron variant A/C;G snv 0.50 2
rs6545817
BCL11A
1.000 0.080 2 60488044 intron variant C/T snv 0.49 2