Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 6
rs6906846
HLA-B ; USP8P1
0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 6
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 4
rs2254556 0.851 0.280 6 31374854 intron variant T/C snv 0.85 3
rs1564267 0.925 0.160 8 11480378 non coding transcript exon variant T/A;C;G snv 2
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 2
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 2
rs3129860 0.925 0.240 6 32433302 intergenic variant A/G;T snv 2
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 2
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs2618476
BLK
0.925 0.160 8 11495032 intron variant T/C snv 0.26 2
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 2
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 2
rs12068753 1.000 0.120 1 159722747 intergenic variant T/A snv 0.15 1
rs13256690 1.000 0.120 8 11481059 non coding transcript exon variant G/A;C;T snv 1
rs1531577 1.000 0.120 8 11481052 non coding transcript exon variant C/T snv 0.71 1
rs17416878 1.000 0.120 1 16120485 downstream gene variant A/G snv 0.24 1
rs2061831 0.925 0.160 8 11482373 upstream gene variant T/C snv 0.25 1
rs2244234 1.000 0.120 8 11478958 upstream gene variant T/G snv 0.83 1
rs2254891 1.000 0.120 8 11483620 upstream gene variant G/A;C snv 1
rs2409780 1.000 0.120 8 11480078 intron variant T/C snv 0.25 1