Disease: Carcinogenesis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121917739
RAD51
0.882 0.080 15 40718818 missense variant G/A snv 3.7E-04 1.7E-03 4
rs1285136498
NR3C1
0.807 0.080 5 143400101 missense variant G/A snv 13
rs17822931
ABCC11
0.827 0.080 16 48224287 missense variant C/G;T snv 4.0E-06; 0.22 0.13 7
rs188957694
ESR1
0.882 0.080 6 151944218 missense variant G/A;C snv 4.0E-05 4.9E-05 6
rs762292600
ESR1
0.925 0.080 6 151944316 missense variant A/G snv 4.0E-06 1.4E-05 7
rs765189442
ABCB11
0.925 0.080 2 168995422 missense variant T/C snv 8.1E-06 4
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs3136797
POLB
0.827 0.120 8 42369287 missense variant C/G snv 1.1E-02 1.1E-02 10
rs6504950
STXBP4
0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs779196500
TP53
0.882 0.120 17 7675187 missense variant G/A snv 4.0E-06 5
rs11283943
MCC
0.882 0.160 5 113071088 splice donor variant -/CGCACTGTCTTCCT;CGCGCTGTCTTCCT;CGTGCTGTCTTCCT delins 4
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs763193414
ERBB2
0.827 0.160 17 39707034 missense variant G/A snv 3.7E-05 4.9E-05 7
rs7726159
TERT
0.790 0.160 5 1282204 intron variant C/A snv 0.29 10
rs2229992
APC
0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 6
rs4987188
MSH2
0.790 0.200 2 47416318 missense variant G/A;T snv 1.3E-02; 2.0E-05 11
rs74315364
RNASEL
0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs1190999960
ZNRD2-AS1 ; ZNRD2 ; FAM89B
0.807 0.240 11 65571690 missense variant G/A snv 9
rs1250394819
LOC101927100 ; TMED7-TICAM2 ; TMED7
0.807 0.240 5 115616325 missense variant C/T snv 4.0E-06 9
rs16999593
DNMT1
0.742 0.240 19 10180505 missense variant T/C snv 2.4E-02 9.6E-03 14
rs568887534
DCTN6
0.807 0.240 8 30183156 missense variant A/G snv 4.0E-06 9
rs1047840
EXO1
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs13010627
CASP10
0.807 0.280 2 201209375 missense variant G/A snv 4.2E-02 4.3E-02 10
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2072668
OGG1
0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14