Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000113
IRGM
0.925 0.040 5 150860514 intron variant C/T snv 0.13 1
rs1001007
CCR5AS
0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs1004234
LINC02863 ; IRF1-AS1
0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 1
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs10051722 1.000 0.040 5 130768383 intron variant A/C;G snv 2
rs10065637
ANKRD55
1.000 0.040 5 56143024 intron variant C/T snv 0.15 2
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 5
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs10181042
PUS10
1.000 0.040 2 60997124 intron variant C/T snv 0.41 1
rs10185424 0.925 0.040 2 102046427 intron variant T/G snv 0.62 2
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv 2
rs10210302
ATG16L1
1.000 0.040 2 233250193 intron variant C/A;T snv 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10276381
JAZF1
1.000 0.040 7 28150502 intron variant C/A;T snv 1
rs1042058
MAP3K8
1.000 0.040 10 30439172 synonymous variant T/C snv 0.51 0.45 2
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 2
rs10486483
SKAP2
1.000 0.040 7 26852821 intron variant G/A snv 0.21 2
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 2
rs10492862
CDH13
1.000 0.040 16 82833851 intron variant C/A;G;T snv 1
rs1049526
BRD2
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 3
rs10495903
THADA
1.000 0.040 2 43579779 intron variant C/T snv 0.13 2
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15 5
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 1