Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1669539 1.000 0.080 2 105998818 intergenic variant T/C snv 7.1E-02 2
rs146893001
PTPN3
1.000 0.080 9 109419337 intron variant T/C snv 3.9E-03 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs1318772
MCC
1.000 0.080 5 113387870 intron variant A/G snv 0.18 2
rs7952106 1.000 0.080 11 113553836 regulatory region variant G/T snv 0.71 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs3115229 1.000 0.080 4 122088578 upstream gene variant T/C snv 9.9E-03 1
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 4
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs543023132 1.000 0.080 6 155652652 downstream gene variant TTTTT/-;T;TT;TTT;TTTT;TTTTTT;TTTTTTT delins 0.12 1
rs75853687
LINC01847
0.925 0.080 5 159850278 intron variant G/A snv 1.7E-02 2
rs9714060
MUC4
1.000 0.080 3 195760605 intron variant A/C;G snv 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 8
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs2445284 1.000 0.080 11 5008473 downstream gene variant C/T snv 0.57 1
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs33930165
HBB
0.882 0.120 11 5227003 missense variant C/G;T snv 9.2E-04; 4.4E-05 1
rs7216169
RABEP1
1.000 0.080 17 5316216 intron variant C/T snv 0.12 1
rs7948471
HBE1 ; HBG2 ; OR51B5 ; OR51I2
1.000 0.080 11 5450516 intron variant G/A snv 0.47 1