Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999885
AP4M1 ; MCM7
0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 3
rs9970827 1.000 0.080 1 185409746 regulatory region variant G/A snv 0.37 1
rs9967368
TYMS ; TYMSOS
1.000 0.080 18 656020 intron variant C/G;T snv 1
rs9966765
LOC107985182 ; MIR122
1.000 0.080 18 58449558 non coding transcript exon variant C/G;T snv 1
rs9926344
WWOX
1.000 0.080 16 78986883 intron variant G/A;C;T snv 2
rs9912300
ACLY
0.827 0.120 17 41869011 intron variant G/A;C;T snv 4.2E-06; 0.78 5
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs988574
ITGA1
1.000 0.080 5 52944980 missense variant A/G snv 5.5E-02 8.6E-02 1
rs9877457 1.000 0.080 3 135564539 intergenic variant A/G;T snv 1
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs975263
MACC1
0.827 0.120 7 20158817 stop gained G/A;T snv 0.34 7
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv 3
rs9679162
GALNT14
0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs964372
MT1B
0.925 0.160 16 56652118 intron variant C/G;T snv 2
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 9
rs9619311
TIMP3 ; SYN3
0.851 0.160 22 32800707 intron variant T/C snv 0.40 4
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs9485372
TAB2
0.807 0.120 6 149287738 intron variant G/A snv 0.20 6
rs947345
MEGF6
1.000 0.080 1 3507824 missense variant G/A snv 4.7E-02 6.1E-02 1
rs9434711
CHD5
1.000 0.080 1 6151123 missense variant G/A;C snv 0.37; 4.0E-06 1
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs9397984
ARID1B
1.000 0.080 6 156898551 intron variant T/C snv 0.14 1
rs9383951
ESR1
1.000 0.080 6 151974478 intron variant G/C snv 5.1E-02 1