Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3024994
VEGFA
0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs2498801
LOC102723342 ; AKT1
0.790 0.120 14 104769221 upstream gene variant T/C snv 0.41 7
rs937475913
PRKDC
0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7
rs11191439
AS3MT ; BORCS7-ASMT
0.851 0.120 10 102878966 missense variant T/A;C snv 9.2E-02 6
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 6
rs11892031
UGT1A10 ; UGT1A8
0.882 0.120 2 233656637 intron variant A/C;T snv 5
rs2292016
OSMR-AS1 ; OSMR
0.851 0.120 5 38845758 non coding transcript exon variant G/T snv 1.9E-02 5
rs3218373
XRCC2
0.827 0.120 7 152677078 upstream gene variant C/A snv 0.15 5
rs587783064
TP53
0.851 0.120 17 7669626 missense variant C/A;T snv 5
rs779682021
CYP1A1
0.882 0.120 15 74721227 missense variant A/C snv 5
rs887569
EZH2
0.882 0.120 7 148808210 intron variant C/T snv 0.73 5
rs10743980
LRP6
0.882 0.120 12 12259861 intron variant T/A;C;G snv 4
rs2073859
LIMK2
0.882 0.120 22 31278567 3 prime UTR variant G/A snv 4.0E-02 4
rs2278329
OSMR
0.851 0.120 5 38921686 missense variant G/A snv 3.3E-02 2.2E-02 4
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 3
rs10234749 0.882 0.120 7 152690784 regulatory region variant T/C;G snv 3
rs10775480
LOC105372093 ; SLC14A1
0.882 0.120 18 45737317 intron variant T/C snv 0.61 3
rs11077654
SLC39A11
0.882 0.120 17 73010373 intron variant A/C snv 0.69 3
rs11191438
AS3MT ; BORCS7-ASMT
0.882 0.120 10 102878107 intron variant G/A;C snv 3
rs1135612
POR
0.882 0.120 7 75980359 synonymous variant A/G;T snv 0.28 3
rs11543198
CLK3
0.882 0.120 15 74619987 missense variant G/A;T snv 0.11 3
rs11871756
SLC39A11
0.882 0.120 17 72730105 intron variant C/G snv 0.11 3
rs1189516787
CEBPA ; CEBPA-DT
0.882 0.120 19 33301681 missense variant C/G snv 7.1E-06 3
rs1203030830
EGFR
0.882 0.120 7 55155873 synonymous variant T/C snv 4.0E-06 3
rs1336331763
SULT1A1
0.882 0.120 16 28606796 missense variant G/A snv 4.0E-06 3