Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2242944 1.000 0.040 21 39093252 intergenic variant G/A snv 0.46 1
rs2394250
HLA-A ; HCG9
1.000 0.040 6 29975879 intron variant G/T snv 0.40 1
rs2402752 1.000 0.040 7 124799545 regulatory region variant T/A;C snv 1
rs2531875 1.000 0.040 17 27821141 intron variant G/A;T snv 1
rs27434
ERAP1
1.000 0.040 5 96793809 synonymous variant A/G;T snv 0.72; 1.2E-05 1
rs27529
ERAP1
1.000 0.040 5 96790605 missense variant A/G;T snv 0.62 1
rs3750996
STIM1
1.000 0.040 11 4091970 3 prime UTR variant A/G snv 7.7E-03 1
rs378108 1.000 0.040 21 39097594 intergenic variant A/G snv 0.42 1
rs41299637
INAVA
1.000 0.040 1 200908722 splice region variant T/A;G snv 0.20 1
rs4333130
ANTXR2
1.000 0.040 4 80028675 intron variant C/G;T snv 1
rs4349859
MICA-AS1
0.925 0.040 6 31398010 upstream gene variant G/A snv 3.1E-02 1
rs4389526
ANTXR2
1.000 0.040 4 80025321 intron variant T/A snv 0.59 1
rs4552569 1.000 0.040 5 83877774 upstream gene variant C/T snv 0.75 1
rs6502398 1.000 0.040 17 14832175 upstream gene variant A/C;T snv 1
rs6759298 1.000 0.040 2 62341310 regulatory region variant G/A;C snv 1
rs7217335
NOS2
1.000 0.040 17 27771755 intron variant G/A snv 0.17 1
rs769178 1.000 0.040 6 31579737 downstream gene variant G/T snv 8.3E-02 1
rs7743761 1.000 0.040 6 31368323 intron variant C/A snv 0.31 1
rs8176786
NELL1
0.925 0.040 11 20937848 missense variant C/T snv 4.5E-02 3.7E-02 1
rs9438876
RUNX3
1.000 0.040 1 24914625 intron variant A/G snv 0.53 1
rs7282490
GATD3A
0.882 0.080 21 44195858 intron variant G/A;T snv 4
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 3
rs115879499 0.925 0.080 6 31392512 downstream gene variant A/G snv 2
rs116488202 0.882 0.080 6 31377139 upstream gene variant C/A;T snv 2
rs2310173 0.925 0.080 2 102047167 intron variant T/C;G snv 2