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
rs4921483
LOC285626
1.000 0.080 5 159341357 intron variant A/G snv 0.89 1
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs354528
SLC16A10
1.000 0.080 6 111184068 intron variant C/T snv 0.76 1
rs27044
ERAP1 ; LOC102724748
0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 1
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
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 1
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs4655683
IL23R ; C1orf141
1.000 0.080 1 67145930 intron variant G/A snv 0.37 1
rs702873
LINC01185
0.882 0.120 2 60854407 intron variant C/T snv 0.35 2
rs13017599
NONOP2
0.882 0.160 2 60937196 non coding transcript exon variant G/A snv 0.25 2
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 2
rs1610601
HLA-F-AS1 ; HLA-F
1.000 0.080 6 29732406 intron variant C/A;T snv 0.20 1
rs2621322 1.000 0.080 6 32820935 intron variant T/G snv 0.20 1
rs4683946 0.925 0.080 3 101896982 intron variant G/T snv 0.19 2
rs12356475
CTNNA3
1.000 0.080 10 66001962 intron variant T/C snv 0.15 1
rs13191343
HLA-C ; HLA-B
1.000 0.080 6 31273332 intron variant C/G;T snv 0.13 1
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 2
rs9378127
HLA-DMA
1.000 0.080 6 32954682 intron variant G/A snv 0.11 1
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 1