Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 5
rs112607182 3 170309619 downstream gene variant C/T snv 5.3E-02 2
rs17158386 7 29765745 regulatory region variant G/A snv 0.19 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
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
rs16943246 15 45428399 upstream gene variant G/A snv 0.29 1
rs185291443 2 226120788 intergenic variant C/A;G snv 1
rs35311980 2 228295484 intergenic variant C/T snv 4.9E-05 1
rs35924503 2 228266570 intergenic variant T/C snv 1.5E-04 1
rs4288924 14 68835682 intergenic variant G/A;T snv 1
rs6712846 2 207024356 intergenic variant G/A snv 0.53 1
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
rs11162351
AK5
1 77479047 intron variant C/G snv 0.31 1
rs144994089
AQP7
9 33385158 missense variant C/T snv 7.0E-04 8.2E-04 1
rs702634
ARL15
1.000 0.080 5 53975590 intron variant G/A snv 0.72 3
rs34823645
C2orf83
2 227647210 intron variant T/C snv 3.9E-04 1
rs2601006
CCT2 ; MIR3913-1
12 69585737 5 prime UTR variant C/T snv 0.39 1
rs4738817
CHD7
8 60708054 intron variant G/A snv 0.36 1
rs35483183
COL4A4
2 227011971 intron variant G/A snv 8.4E-02 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25