Source: GWASCAT ×
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 23
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 7
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 6
rs4976646
RGS14
0.851 0.200 5 177361569 intron variant T/C snv 0.41 6
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 5
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 5
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 5
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 5
rs1534422
MIR3681HG
0.827 0.160 2 12500615 intron variant G/A snv 0.52 4
rs17119
LOC101928354
0.882 0.120 6 14719265 intron variant G/A snv 0.74 4
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs2777899
VMP1
0.851 0.160 17 59755030 intron variant T/A;G snv 4
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 4