Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs4859584
ART3 ; CXCL10
1.000 0.040 4 76021984 intron variant G/C snv 0.61 0.61 1
rs5745568
GGNBP1 ; BAK1
0.882 0.080 6 33580617 intron variant G/T snv 0.19 4
rs6065
CHRNE ; GP1BA
0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 6
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 4
rs669260
DDX58
0.851 0.080 9 32503442 intron variant T/A;C snv 4
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
rs750898115
USO1
0.882 0.080 4 75787191 missense variant A/G snv 1.0E-05 3.5E-05 4
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19