Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 38
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs397507545
PTPN11
0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 16
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 13
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 10
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 9
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 9
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 8
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 6
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 6
rs2534657
MICB
0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 5
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 5
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs2516513
MICB-DT
0.925 0.120 6 31479811 downstream gene variant C/T snv 0.20 5