Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999788
IL10RB ; IL10RB-DT ; IFNAR2
0.925 0.120 21 33265726 non coding transcript exon variant C/T snv 0.20 2
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs9934438
VKORC1
1.000 0.080 16 31093557 5 prime UTR variant G/A;C snv 1
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs9923231
VKORC1
0.851 0.200 16 31096368 upstream gene variant C/A;G;T snv 6
rs9899375
CHD3
1.000 0.080 17 7908297 intron variant C/T snv 8.1E-03 2
rs9860747 0.925 0.080 3 186869628 regulatory region variant T/C snv 0.70 2
rs982873 0.925 0.160 13 90145678 intergenic variant T/C snv 0.65 2
rs980857256
ACE
1.000 0.080 17 63485015 stop gained C/T snv 8.2E-06 6.3E-05 1
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs978906
ROCK2
0.925 0.080 2 11183150 3 prime UTR variant T/A;C snv 3
rs9722
S100B
0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21 9
rs9662221
SLC26A9-AS1
1.000 0.080 1 205946617 upstream gene variant G/T snv 0.32 1
rs966221
PDE4D
1.000 0.080 5 60206693 intron variant A/G snv 0.57 2
rs9657362
ARHGEF10
0.882 0.120 8 1885635 missense variant G/C;T snv 0.16 3
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs9574
PROCR ; MMP24-AS1-EDEM2
1.000 0.080 20 35176829 3 prime UTR variant C/A;G;T snv 1.1E-03; 0.55 2
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs9534275
BRCA2
0.851 0.080 13 32366208 intron variant C/A snv 0.52 7
rs9533290 1.000 0.080 13 30863403 intergenic variant A/G snv 0.64 1
rs9533156
TNFSF11
0.807 0.280 13 42573535 intron variant T/C snv 0.47 8
rs9526212
LRCH1
1.000 0.080 13 46651610 intron variant A/G snv 0.74 2
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 3
rs9333358
IFNB1
1.000 0.080 9 21078953 upstream gene variant T/C snv 0.20 1
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8