Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs2534657
MICB
0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 5
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 5
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs2516513
MICB-DT
0.925 0.120 6 31479811 downstream gene variant C/T snv 0.20 5
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 4
rs2763979
HSPA1B
0.827 0.360 6 31826815 upstream gene variant C/T snv 0.45 3
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 3
rs2734986
LOC105375010
0.827 0.160 6 29850791 intron variant T/C snv 0.10 3
rs805294
LY6G6C ; MPIG6B
0.882 0.240 6 31720440 intron variant A/G snv 0.48 3
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 3
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3