Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs735239
CD209
0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs3739319
IDO1
0.925 0.040 8 39927802 intron variant G/A snv 0.40 0.37 2
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs1285933
CLEC5A ; MGAM
0.925 0.040 7 141927349 intron variant G/A snv 0.54 2
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs4859584
ART3 ; CXCL10
1.000 0.040 4 76021984 intron variant G/C snv 0.61 0.61 1
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3132468
MICB
0.827 0.240 6 31507709 intron variant C/T snv 0.77 5
rs2285932
OAS3
0.851 0.120 12 112949145 synonymous variant T/C snv 0.76 0.78 5