Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs34779708
CREM
0.827 0.120 10 35177257 intron variant T/G snv 0.33 6
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs6425143 0.827 0.120 1 172875212 intron variant T/G snv 0.34 5
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 5
rs6720394
MIR4435-2HG
0.925 0.040 2 111231795 intron variant T/G snv 0.11 1
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs4921482
LOC285626
0.807 0.120 5 159337470 intron variant T/C;G snv 6
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv 6
rs1333062
ITLN1
0.807 0.200 1 160876494 downstream gene variant T/C;G snv 5
rs73178598
LOC105376976
0.827 0.120 3 18763719 intron variant T/C;G snv 5
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
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
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 6