Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 12
rs2186607
TRPC6
0.776 0.080 11 101785666 intron variant T/A snv 0.51 10
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs230490
LOC105377621
0.882 0.080 4 102466262 downstream gene variant G/A snv 0.34 3
rs4648110
NFKB1 ; LOC105377347
0.925 0.080 4 102612664 intron variant T/A snv 0.22 3
rs997476 0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02 3
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12 9
rs750521832
MMP8
0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs4919687
CYP17A1
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 14
rs12548629
BAALC ; BAALC-AS1
0.776 0.120 8 103189173 intron variant C/T snv 0.24 10
rs7911488
MIR1307 ; ATP5MD
0.882 0.080 10 103394332 5 prime UTR variant A/G snv 0.34 0.26 3
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs4135113
TDG
0.925 0.080 12 103982915 missense variant G/A;C;T snv 4.7E-02 5
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs17035289 0.790 0.080 4 105127134 intergenic variant T/C snv 0.25 9
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs17035310 0.790 0.080 4 105143597 upstream gene variant C/T snv 0.14 10
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs6928864 0.790 0.080 6 105519019 intron variant C/A;T snv 9
rs1512436 0.790 0.080 11 106436144 intergenic variant T/C snv 0.50 10
rs1383147053
DLD
0.882 0.120 7 107901762 missense variant G/A snv 4
rs1078643
TMEM220-AS1 ; TMEM238L
0.776 0.080 17 10803924 missense variant G/A;C snv 10
rs1364898025
ATM
0.925 0.080 11 108227656 missense variant G/A snv 3
rs9583269
MYO16
0.790 0.080 13 108630682 intron variant C/T snv 0.34 9