Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1388585 12 40137889 downstream gene variant G/A snv 0.95 1
rs1049526
BRD2
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs2395022
KPNA7
7 99152756 intergenic variant A/C snv 0.93 1
rs9313808 5 159393836 intron variant A/G snv 0.89 1
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 5
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 1
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 5
rs2847278 18 12778716 upstream gene variant C/T snv 0.83 1
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 2
rs2328546
CDKAL1
6 20657114 intron variant T/C snv 0.81 1
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 3
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs6708413
IL18RAP
1.000 0.040 2 102446909 intron variant G/A snv 0.78 2
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 1
rs6740462
LOC105374780
1.000 0.040 2 65440138 intron variant C/A snv 0.78 2
rs8009169 14 42813211 intergenic variant G/C snv 0.78 1
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 6
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs130555
SYN3
1.000 0.040 22 32787803 intron variant C/T snv 0.77 2
rs3116494
CD28
0.882 0.120 2 203727298 intron variant G/A snv 0.76 2
rs4552569 1.000 0.040 5 83877774 upstream gene variant C/T snv 0.75 1
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 1