Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5