Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 4
rs10098821
LINC00824
0.882 0.120 8 128546982 intron variant C/T snv 7.6E-02 3
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1046428
GSTZ1
0.776 0.200 14 77327940 missense variant T/A;C snv 4.0E-06; 0.81 8
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519865
FOXL2NB ; FOXL2
0.742 0.240 3 138946321 missense variant G/C snv 15
rs1064795649
BRIP1
1.000 0.120 17 61799205 frameshift variant CT/- delins 2
rs10756819
BNC2
1.000 0.120 9 16858086 intron variant G/A;C;T snv 1
rs10810666 1.000 0.120 9 16911668 intergenic variant C/T snv 0.14 1
rs10962656 1.000 0.120 9 16877790 intergenic variant G/A snv 0.10 1
rs11084033
LOC105372441
0.882 0.120 19 50850699 intron variant C/A;T snv 4
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
rs1131691022
TP53
0.827 0.160 17 7670685 frameshift variant GG/A;G delins 6