Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141095230
MGMT
0.925 0.120 10 129536277 missense variant C/A;T snv 8.0E-06; 5.2E-05 2
rs1412335442
PIK3CG
0.925 0.120 7 106868317 missense variant G/T snv 7.0E-06 2
rs1448106115
PMS2
0.925 0.120 7 5989944 missense variant T/C snv 4.0E-06 2
rs145574072
OGG1
0.925 0.120 3 9754765 synonymous variant T/C snv 4.0E-06 2
rs145733073
UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A10
0.925 0.120 2 233682175 missense variant T/C;G snv 4.0E-06; 1.4E-04 2
rs149243735
OGG1
0.925 0.120 3 9751076 missense variant C/A snv 4.0E-06 2
rs1547374
LOC105372815
0.925 0.120 21 42358786 downstream gene variant A/G snv 0.32 2
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs1630747
SLC5A3 ; MRPS6
0.925 0.120 21 34085692 intron variant C/A snv 0.69 2
rs17458086
SLC2A13
0.925 0.120 12 40034837 intron variant T/C snv 1.1E-02 2
rs17884306
TP53
0.925 0.120 17 7668783 3 prime UTR variant C/T snv 5.1E-02 2
rs1800843
CCKBR
0.925 0.120 11 6270835 synonymous variant C/A;G snv 0.16; 4.0E-06 0.19 2
rs1810205
CUBN
0.925 0.120 10 16923228 intron variant A/G snv 0.47 2
rs199474357
HLA-A
0.925 0.120 6 29942790 missense variant T/C;G snv 2
rs200349340
HOTAIR
0.925 0.120 12 53962704 non coding transcript exon variant T/A;G snv 2
rs201753355
HTATSF1P2 ; NQO2
0.925 0.120 6 3019647 missense variant G/A;C snv 2.0E-05 2
rs2073389
SMARCB1
0.925 0.120 22 23791306 intron variant C/T snv 0.59 2
rs2074733
SF3A1
0.925 0.120 22 30342598 non coding transcript exon variant T/C snv 0.53 2
rs2255280
C9 ; DAB2
0.925 0.120 5 39394887 intron variant C/A snv 0.98 2
rs2457571
SLC22A3
0.925 0.120 6 160413796 intron variant T/C snv 0.62 2
rs2470353
XPC ; LOC107986063
0.925 0.120 3 14148768 intron variant G/A;C;T snv 0.41; 1.5E-04 2
rs2980874
TRIB1
0.925 0.120 8 125432546 intron variant G/A snv 0.30 2
rs3021088
ND2 ; COX1
0.925 0.120 MT 5460 missense variant G/A snv 2
rs3124761
SLC2A6
0.925 0.120 9 133474633 intron variant T/C snv 0.80 2
rs34852782
PRKAG2
0.925 0.120 7 151869086 intron variant -/A;AG ins 2