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
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 3
rs12044149
C1orf141
0.925 0.080 1 67135003 intron variant G/C;T snv 1
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 1
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 1
rs4655683
IL23R ; C1orf141
1.000 0.080 1 67145930 intron variant G/A snv 0.37 1
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs13017599
NONOP2
0.882 0.160 2 60937196 non coding transcript exon variant G/A snv 0.25 2
rs702873
LINC01185
0.882 0.120 2 60854407 intron variant C/T snv 0.35 2
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs4683946 0.925 0.080 3 101896982 intron variant G/T snv 0.19 2
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs4921482
LOC285626
0.807 0.120 5 159337470 intron variant T/C;G snv 6
rs74817271
TNIP1
0.807 0.120 5 151090412 intron variant G/A snv 5.0E-02 6
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 2
rs2631367
MIR3936HG ; SLC22A5
0.925 0.120 5 132369766 5 prime UTR variant C/G snv 0.59 1
rs27044
ERAP1 ; LOC102724748
0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs4921483
LOC285626
1.000 0.080 5 159341357 intron variant A/G snv 0.89 1
rs76956521
TNIP1
1.000 0.080 5 151085080 intron variant A/C;G snv 1
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 2