Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 3
rs689
INS ; INS-IGF2
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 1
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 3
rs7171171
LOC107984725
0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 1
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 1
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5