Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 7
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 7
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs1329568 0.882 0.120 9 37037979 upstream gene variant T/A;G snv 6
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 6
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 6
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5