Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1001581
XRCC1
1.000 0.080 19 43561236 intron variant C/T snv 0.38 1
rs10023113
CAMK2D
1.000 0.080 4 113625548 intron variant A/G snv 0.18 1
rs1005165
CD3EAP ; PPP1R13L
1.000 0.080 19 45405792 intron variant C/T snv 0.21 1
rs10079250
CSF1R
0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 7
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1022059218
ICOS ; LOC101927840
0.925 0.200 2 203936863 missense variant G/A snv 2
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs1032737355
EGFR
0.925 0.080 7 55170434 missense variant T/A snv 2
rs1042489
BIRC5
0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042852
CBLB
1.000 0.080 3 105658671 3 prime UTR variant C/G;T snv 1
rs10429489 0.925 0.080 9 21787522 intergenic variant G/A snv 0.26 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1046175
PAOX
0.851 0.080 10 133391446 stop gained C/A;G;T snv 1.2E-05; 0.88 4
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1048977
CDA
1.000 0.080 1 20618562 synonymous variant C/T snv 0.31 0.34 2
rs1049434
SLC16A1
0.925 0.120 1 112913924 missense variant A/T snv 0.59 0.66 2
rs1050171
EGFR ; EGFR-AS1
0.851 0.120 7 55181370 missense variant G/A;C snv 0.52; 4.0E-06 6
rs10503380 1.000 0.080 8 9552985 upstream gene variant C/T snv 0.25 2
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31