Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 2
rs402072
PRKD2
1.000 0.120 19 46715865 intron variant T/C snv 0.12 1
rs425105
PRKD2
0.925 0.160 19 46705224 intron variant T/C snv 0.15 1
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 2
rs727088
CD226
0.790 0.400 18 69863203 3 prime UTR variant G/A snv 0.47 2
rs1615504
CD226
1.000 0.120 18 69859408 3 prime UTR variant T/C snv 0.46 1
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 1
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 3
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 1
rs12453507 0.925 0.200 17 39896954 intergenic variant C/G;T snv 1
rs16956936
DNAH2
1.000 0.120 17 7730374 intron variant C/A;T snv 1
rs2107538
LOC105371744 ; CCL5
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27 1
rs4459609 0.925 0.120 17 63471587 upstream gene variant C/A snv 0.63 1
rs7221109 0.925 0.160 17 40614034 intergenic variant T/C snv 0.69 1
rs757411 1.000 0.120 17 40618898 intergenic variant C/T snv 0.67 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14