Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4844880
HSD11B1-AS1 ; HSD11B1
0.882 0.240 1 209697571 intron variant A/T snv 0.70 4
rs1340420
TNKS2
0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs1770474
TNKS2
0.925 0.080 10 91833770 intron variant G/A;T snv 3
rs181696
PLCH1
0.925 0.080 3 155548315 intron variant T/C snv 0.55 3
rs11466345
TGFB1
1.000 0.080 19 41337556 intron variant T/C snv 0.12 2
rs12541709
TNKS
1.000 0.080 8 9751081 intron variant C/G snv 0.29 2
rs12613347
CASP10
2 201190589 intron variant C/T snv 0.19 1
rs3764221
CYP19A1
15 51296650 intron variant G/A;T snv 1
rs4396880
TP63
3 189638432 intron variant G/A snv 0.34 1
rs8038415
IGF1R
15 98956205 intron variant T/C snv 0.58 1
rs11991621 1.000 0.080 8 9549072 intergenic variant C/T snv 0.18 2
rs17429138
LOC107986169
3 189527804 intergenic variant A/G snv 0.26 1
rs6601328 1.000 0.080 8 9545693 regulatory region variant G/A;C snv 2
rs863225307
APC
5 112819077 stop gained C/T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88