Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 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
rs3094187
CCHCR1 ; TCF19
0.925 0.120 6 31159167 5 prime UTR variant C/T snv 0.55 5
rs3094214
CDSN ; PSORS1C1
0.925 0.120 6 31117605 non coding transcript exon variant C/A snv 0.58 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs540385376
PSORS1C1 ; CDSN
0.925 0.120 6 31117605 non coding transcript exon variant C/A snv 5
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 3
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 3
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 3
rs907091
IKZF3
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 3