Source: GWASDB

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
rs1002922 1.000 0.040 5 40386453 regulatory region variant T/C snv 0.29 1
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs10065637
ANKRD55
1.000 0.040 5 56143024 intron variant C/T snv 0.15 1
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 2
rs10117785
TNFSF15
1.000 0.040 9 114789323 3 prime UTR variant T/A snv 0.34 1
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1
rs10181042
PUS10
1.000 0.040 2 60997124 intron variant C/T snv 0.41 1
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv 1
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
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs1042058
MAP3K8
1.000 0.040 10 30439172 synonymous variant T/C snv 0.51 0.45 1
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 1
rs10484545
LOC101929006
1.000 0.040 6 29266733 intron variant C/A;G snv 1
rs10486483
SKAP2
1.000 0.040 7 26852821 intron variant G/A snv 0.21 1
rs10489276 1.000 0.040 1 172893799 intron variant C/T snv 0.31 1
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 1
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
rs10512734 1.000 0.040 5 40393503 intergenic variant A/C;G snv 0.29 1
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 2
rs10734105 1.000 0.040 10 131373856 intergenic variant G/A;C;T snv 1
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5