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
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs6065
CHRNE ; GP1BA
0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 6
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs750898115
USO1
0.882 0.080 4 75787191 missense variant A/G snv 1.0E-05 3.5E-05 4
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
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
rs371057322
KIDINS220
0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 2
rs3740360
PLCE1
0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 7
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs1447043692
HPSE2
0.925 0.040 10 98641918 missense variant C/T snv 2