Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
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
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
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 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
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5