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
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs2974935
MTX1
0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs4360494
SF3A3
0.776 0.080 1 37990219 upstream gene variant G/C snv 0.45 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 11
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 10
rs6678517
LAMC1
0.776 0.080 1 183033504 intron variant A/G;T snv 10
rs17011141
LINC02257
0.776 0.080 1 221939292 intron variant A/G snv 0.21 10
rs12144319
TTC22
0.776 0.080 1 54780362 3 prime UTR variant T/C snv 0.31 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9