Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs13397
MIR3202-2 ; TMEM187
0.925 0.200 X 153982797 synonymous variant G/A snv 0.27 0.15 2
rs5979785 0.925 0.160 X 12953405 intergenic variant C/T snv 1
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 3
rs4821124 0.851 0.240 22 21625000 downstream gene variant T/C snv 0.19 3
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 1
rs58911644
GATD3A ; LOC107983952 ; LOC102725065
1.000 0.080 21 44209238 3 prime UTR variant A/T snv 1
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs6032606
ZNF335
1.000 0.080 20 45967568 missense variant C/A;G snv 0.84 1
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
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
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs80209296
PTPN2
0.925 0.200 18 12860802 intron variant G/A snv 2
rs11875687
PTPN2
1.000 0.080 18 12843138 intron variant T/C snv 0.17 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
rs2074404
LRRC37A2 ; WNT3
0.925 0.120 17 46788073 intron variant T/G snv 0.27 2