Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs2187670 1.000 0.080 3 46325463 intergenic variant T/C snv 0.81 1
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 3
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 1
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs6498114
CIITA ; LOC105371080
1.000 0.080 16 10870261 intron variant G/T snv 0.78 2
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs6441961
UQCRC2P1
1.000 0.080 3 46310893 non coding transcript exon variant T/C snv 0.74 1
rs2474619
BACH2
0.882 0.360 6 90170316 intron variant C/A snv 0.72 1
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs2097282 1.000 0.080 3 46336534 intergenic variant C/T snv 0.68 1
rs7100025
ANKRD30A ; LINC00993
0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs936229
ULK3
1.000 0.080 15 74839978 intron variant A/G snv 0.67 1
rs212402
LOC105378083
1.000 0.080 6 159051263 intron variant G/A snv 0.66 1
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 1
rs212400
LOC105378083
0.925 0.200 6 159052542 non coding transcript exon variant A/G snv 0.64 2
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs1250557
ZMIZ1
1.000 0.080 10 79306017 intron variant G/T snv 0.63 1
rs7616215
CCR3 ; LOC105377067
0.925 0.280 3 46164194 intron variant C/T snv 0.62 2
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 1
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs4128561
ETS1
1.000 0.080 11 128545234 intron variant T/C snv 0.58 1