Source: GWASDB

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 13
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 3
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 3
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs7554511
INAVA
0.925 0.040 1 200908434 intron variant C/A snv 0.22 3
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 2
rs2297909
KIF21B
0.925 0.080 1 200991179 intron variant G/A snv 0.27 0.27 2
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 2
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 2
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs10489276 1.000 0.040 1 172893799 intron variant C/T snv 0.31 1