Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
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
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 4
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 4
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48 4
rs1534422
MIR3681HG
0.827 0.160 2 12500615 intron variant G/A snv 0.52 4
rs11571297 0.882 0.120 2 203880280 regulatory region variant T/C snv 0.44 3
rs231726 0.790 0.200 2 203876143 downstream gene variant C/T snv 0.36 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 3
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 3