Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10065633
IRF1-AS1
1.000 0.040 5 132481024 intron variant T/C snv 0.38 1
rs10251201
UMAD1
0.851 0.160 7 7932654 intron variant T/A;C snv 4
rs10405859
PPP1R37 ; MARK4
0.882 0.080 19 45099523 intron variant T/C snv 0.48 3
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894421
LIG4
0.882 0.200 13 108210436 missense variant C/A;T snv 1.2E-05 4
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs1057519766
FLT3
0.851 0.080 13 28028203 missense variant G/C;T snv 5
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs10931910
AOX1
0.925 0.040 2 200659013 intron variant A/G;T snv 2
rs11079041
STAT5B
0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 4
rs113017087
APC
1.000 0.040 5 112737780 intron variant T/C snv 5.4E-03 1
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11545078
GGH
0.807 0.200 8 63026205 missense variant G/A snv 8.8E-02 7.8E-02 6
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs115658307
APC
1.000 0.040 5 112707537 5 prime UTR variant C/T snv 4.8E-03 1
rs1188975135
APOBEC3C ; APOBEC3F
0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 4
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121434629
PMS2
0.763 0.320 7 6005918 missense variant C/A;T snv 1.6E-04; 8.1E-06 13