Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10108511
LINC00208
0.925 0.080 8 11578007 non coding transcript exon variant T/A;C snv 2
rs1035142
FLACC1
0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 7
rs10419226
CRTC1
0.925 0.080 19 18692362 intron variant T/G snv 0.67 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1059536
HLA-A
1.000 0.080 6 29943448 missense variant A/C;G;T snv 4.1E-06; 0.17 3
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs11775256
TNFRSF10A
1.000 0.080 8 23193972 intron variant C/T snv 0.21 1
rs11789015
BARX1
0.882 0.080 9 93953746 intron variant A/C;G snv 6
rs11901649
APOB
0.882 0.080 2 21027351 intron variant G/A;C;T snv 3
rs11941492
KDR
1.000 0.080 4 55112043 intron variant C/T snv 0.24 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12465911 0.925 0.080 2 150929228 intergenic variant C/T snv 0.21 2
rs1247942 0.925 0.080 12 114235918 downstream gene variant G/A;C snv 2
rs1263178238
VSIG10L
0.925 0.080 19 51338047 missense variant T/C snv 2.6E-05 4.9E-05 2
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs13396805 0.925 0.080 2 150964998 intergenic variant C/T snv 0.20 2
rs13429103
LOC107985847
1.000 0.080 2 7377100 intergenic variant G/A snv 0.16 1
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs17002540 1.000 0.080 X 140863896 intergenic variant C/T snv 0.20 1
rs17451754
CFTR
0.925 0.080 7 117616658 intron variant G/A snv 0.10 2
rs17619601
FLT1
1.000 0.080 13 28326373 intron variant C/T snv 5.0E-02 1
rs17625898
FLT1
1.000 0.080 13 28358693 intron variant T/A;G snv 1
rs17708574
PDGFRB
1.000 0.080 5 150141675 intron variant G/A snv 8.2E-02 1
rs17749155
MSRA
0.925 0.080 8 10210563 intron variant G/A snv 0.16 2