Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 1
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 1
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 2
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 1
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs1320344
C12orf42
0.882 12 103493699 intron variant A/G snv 0.64 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 5
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 1
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 1
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs56817615
CLNK
0.882 4 10717222 intergenic variant A/G snv 0.42 4
rs2108225 1.000 0.040 7 107812658 downstream gene variant G/A;T snv 1
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs374039502
TNFSF13B
0.925 0.160 13 108308037 3 prime UTR variant T/A snv 2.0E-02 1
rs28583049
LOC105374033
0.882 3 108724568 downstream gene variant T/C snv 0.17 4
rs6498142
CLEC16A
16 10987392 intron variant C/G snv 0.77 1