Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
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
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs2900180
C5-OT1
0.827 0.280 9 120944104 regulatory region variant T/A;C snv 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs733361 1.000 0.120 12 125861206 intron variant T/G snv 0.44 1
rs929423 1.000 0.120 12 125862468 intron variant T/C snv 0.44 1
rs4301434
SLA ; TG
1.000 0.120 8 133075205 intron variant A/G snv 0.43 1
rs2294025
TG
1.000 0.120 8 133133268 intron variant G/A snv 0.49 1
rs4736437 1.000 0.120 8 133173424 intergenic variant T/G snv 0.48 1
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs610604
TNFAIP3
0.827 0.240 6 137878280 intron variant G/T snv 0.58 2
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 1
rs3811035
FCRL5
1.000 0.120 1 157515771 splice region variant G/A snv 0.63 0.51 1
rs10908583 1.000 0.120 1 157671893 downstream gene variant C/T snv 0.57 1
rs2210911 1.000 0.120 1 157674077 downstream gene variant A/G snv 0.46 1
rs7522061
FCRL3
0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51 1
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 1
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs12743184 1.000 0.120 1 157784569 intergenic variant A/G snv 0.21 1
rs2050568
FCRL1
0.925 0.160 1 157800451 intron variant C/T snv 0.57 1
rs6689427
FCRL1
1.000 0.120 1 157811102 intron variant A/G snv 0.44 1
rs2765493
CD5L
1.000 0.120 1 157828210 downstream gene variant G/A snv 0.41 1