Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs9277535
HLA-DPB1
0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 4
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 3
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 3
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 3
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 3
rs1794275 1.000 0.120 6 32703471 downstream gene variant G/A snv 0.21 2
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 2
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 2
rs2523946
HCG9 ; HLA-A
0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv 2
rs1883414
HLA-DPB2
0.925 0.200 6 33118671 non coding transcript exon variant G/A snv 0.28 2
rs3803800
TNFSF13 ; TNFSF12-TNFSF13
0.807 0.240 17 7559652 missense variant A/G snv 0.70 0.64 2
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 2
rs2738048 1.000 0.120 8 6965263 downstream gene variant A/G snv 0.28 1
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 1
rs4849121
ACOXL
0.925 0.160 2 110842129 intron variant G/A snv 0.44 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
rs372883
BACH1
0.827 0.360 21 29345416 3 prime UTR variant T/C snv 0.53 1
rs11264794
FCRL3
1.000 0.120 1 157677999 3 prime UTR variant C/A snv 0.63 1
rs7522061
FCRL3
0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51 1
rs2412971
HORMAD2
0.882 0.320 22 30098382 intron variant G/A snv 0.55 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs11574637
ITGAX
0.882 0.200 16 31357553 missense variant T/C snv 0.21 1