Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs2382817
PNKD ; TMBIM1
0.925 0.040 2 218286495 5 prime UTR variant A/C snv 0.61 3
rs6017342
LINC01620
0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 2
rs7165170
CRTC3-AS1 ; CRTC3
1.000 0.040 15 90638257 non coding transcript exon variant A/C snv 0.26 2
rs2395022
KPNA7
7 99152756 intergenic variant A/C snv 0.93 1
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs10051722 1.000 0.040 5 130768383 intron variant A/C;G snv 2
rs10142466 14 68805067 intergenic variant A/C;G;T snv 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 6
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3