Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs2305160
NPAS2 ; NPAS2-AS1
0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7
rs3803800
TNFSF13 ; TNFSF12-TNFSF13
0.807 0.240 17 7559652 missense variant A/G snv 0.70 0.64 7
rs17483466
MIR4435-2HG ; ACOXL
0.827 0.280 2 111039881 intron variant A/G snv 0.15 5
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 5
rs12711846
MIR4435-2HG ; ACOXL-AS1 ; ACOXL
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26 4
rs13069553 0.851 0.200 3 169790484 upstream gene variant A/G snv 0.21 4
rs2720680
PVT1
0.851 0.160 8 128102971 intron variant A/G snv 0.33 4
rs3755397
FARP2
0.925 0.120 2 241355498 upstream gene variant A/G snv 6.8E-02 4
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67 4
rs73005220
CIB3
0.851 0.160 19 16161878 intron variant A/G snv 3.9E-02 4
rs9391997
IRF4
0.851 0.160 6 409119 3 prime UTR variant A/G snv 0.38 4
rs1982809
BTLA ; LOC112268446
0.882 0.200 3 112463893 downstream gene variant A/G snv 0.28 3
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 3
rs35923643
GRAMD1B
0.925 0.120 11 123484683 intron variant A/G snv 0.15 3
rs11636802
LOC105370831
0.925 0.120 15 56483399 intergenic variant A/G snv 8.0E-02 2
rs1274963
CSRNP1
0.925 0.120 3 39149538 non coding transcript exon variant A/G snv 0.82 2
rs13015798
FAM126B
0.925 0.120 2 201044792 intron variant A/G snv 0.23 2
rs142215530
LOC105370831
0.925 0.120 15 56485493 intergenic variant A/G snv 8.0E-02 2
rs1476569 0.925 0.120 4 113777540 intergenic variant A/G snv 0.34 2