Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 3
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 2
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 1
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 1
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 1
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 11
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 2
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 3
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16