Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112607182 3 170309619 downstream gene variant C/T snv 5.3E-02 2
rs10157710 1 47496019 downstream gene variant C/T snv 0.78 1
rs11264327 1 155122631 downstream gene variant G/A;C;T snv 1
rs2470893
CYP1A1
0.882 0.160 15 74727108 upstream gene variant C/T snv 0.20 4
rs16943246 15 45428399 upstream gene variant G/A snv 0.29 1
rs3759794
LTK
15 41514460 upstream gene variant G/A snv 0.12 1
rs838142
FUT1 ; IZUMO1
19 48748894 3 prime UTR variant A/G snv 0.39 1
rs2601006
CCT2 ; MIR3913-1
12 69585737 5 prime UTR variant C/T snv 0.39 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs10995311
ADO
10 62805174 missense variant C/G snv 0.35 0.31 3
rs2236295
ADO
10 62805132 missense variant G/C;T snv 0.32 2
rs45551835
CUBN
1.000 0.080 10 16890385 missense variant G/A;T snv 1.3E-02; 4.0E-06 2
rs141640975
CUBN
10 16950012 missense variant G/A snv 1.7E-03 1.5E-03 1
rs144360241
CUBN
10 16925418 missense variant T/C snv 5.6E-03 5.3E-03 1
rs144994089
AQP7
9 33385158 missense variant C/T snv 7.0E-04 8.2E-04 1
rs1801239
CUBN
0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 1
rs35572189
MIR3186 ; BAHCC1
17 81451999 missense variant G/A;C snv 0.34 1
rs17158386 7 29765745 regulatory region variant G/A snv 0.19 2
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 5
rs12032996 1 33454985 intergenic variant G/A snv 0.12 1
rs12727104 1 171454028 intergenic variant G/A snv 8.3E-02 1
rs13394343 2 85527219 intergenic variant C/A;T snv 1
rs183131780
LOC105373914 ; LOC107985992
2 225820170 intergenic variant C/T snv 1.0E-03 1
rs185291443 2 226120788 intergenic variant C/A;G snv 1
rs35311980 2 228295484 intergenic variant C/T snv 4.9E-05 1