Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs11614178
IFNG-AS1 ; LOC107984526
0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs1267499
LOC101928354
0.807 0.160 6 14715651 intron variant T/A;C snv 6
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 6
rs12968719
PTPN2
0.827 0.120 18 12879467 intron variant G/A snv 8.5E-02 6
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 6
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 6
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2227551
PLAU
0.827 0.120 10 73909432 intron variant G/C;T snv 6
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 6
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 6
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 6
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6