Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2304240
ICAM3
0.882 0.200 19 10338716 synonymous variant A/G snv 0.81 0.85 4
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs707824
LOC101928354
0.925 0.120 6 14636732 intergenic variant T/C snv 0.74 3
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2231231
AQP3
0.851 0.240 9 33442988 non coding transcript exon variant A/C snv 0.67 0.69 5
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2466571
CD46
0.925 0.120 1 207766701 intron variant G/T snv 0.46 3
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs2227307
CXCL8
0.851 0.240 4 73740952 intron variant T/G snv 0.45 6
rs273429
LOC105375763
8 131467654 intergenic variant C/T snv 0.43 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1042752
POU2AF1
0.925 0.120 11 111352386 3 prime UTR variant A/G snv 0.39 3
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs10494879
IL19
0.925 0.120 1 206778859 intron variant C/A;G snv 0.36 3
rs708486
PTGDR
0.925 0.120 14 52274253 intron variant A/G snv 0.35 3
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs6676671
IL19
0.882 0.160 1 206779403 intron variant T/A snv 0.32 4
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs12289961
OR10Q2P
11 58292720 non coding transcript exon variant C/T snv 0.28 1