Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5912838
LOC107985690
0.925 0.280 X 79241621 intergenic variant A/C snv 2
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 3
rs16975792 0.925 0.280 17 70437584 intergenic variant A/G snv 0.26 2
rs181206
IL27
0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24 2
rs2596449
HCP5 ; HCG26
0.925 0.160 6 31470613 non coding transcript exon variant A/G snv 0.79 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs623011 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 2
rs9263688
PSORS1C1
0.925 0.160 6 31124190 intron variant A/G snv 5.2E-02 2
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 1
rs1230666
MAGI3
0.925 0.200 1 113630788 intron variant A/G snv 0.90 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 1
rs3093024
LOC105378122 ; CCR6
0.882 0.200 6 167119305 non coding transcript exon variant A/G snv 0.61 1
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 1
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 3
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs9394159
ITPR3
1.000 0.120 6 33650385 intron variant A/T snv 0.45 1
rs2474619
BACH2
0.882 0.360 6 90170316 intron variant C/A snv 0.72 1
rs229527
C1QTNF6
0.925 0.160 22 37185445 missense variant C/A;G snv 0.43 2
rs1265883
SLAMF6
1.000 0.120 1 160495121 intron variant C/A;G snv 0.96 1