Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 11
rs611646
ATM
0.882 0.120 11 108306370 intron variant T/A;C snv 3
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs869025212
BAP1
0.827 0.200 3 52403428 frameshift variant G/- delins 6
rs375129361
BAP1
0.925 0.120 3 52408056 missense variant T/A;C snv 4.1E-06 2
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
rs1982809
BTLA ; LOC112268446
0.882 0.200 3 112463893 downstream gene variant A/G snv 0.28 3
rs1800645
CALB1
1.000 0.120 8 90083245 intron variant A/G;T snv 1
rs750380279
CCDC127 ; SDHA
0.851 0.200 5 218357 start lost T/A;C;G snv 8.7E-06; 8.7E-06 6
rs7177
CCND1
1.000 0.120 11 69651347 3 prime UTR variant C/A snv 0.44 2
rs1944129
CCND1
1.000 0.120 11 69639167 upstream gene variant C/G;T snv 1
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs2050462
CSF1
0.925 0.120 1 109930334 3 prime UTR variant T/A;G snv 2
rs333951
CSF1
0.925 0.120 1 109909068 upstream gene variant T/C snv 0.74 2
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs2504106
DAAM2
0.925 0.120 6 39854343 intron variant A/G snv 0.61 2
rs6937133
DAAM2
0.925 0.120 6 39832238 intron variant A/C;G snv 2
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs17037102
DKK2
0.807 0.240 4 106924637 missense variant C/A;T snv 0.15 6
rs3206824
DKK3
0.827 0.160 11 11964514 missense variant T/C snv 0.78 0.78 6
rs2291599
DKK3
0.925 0.120 11 11968352 intron variant T/C snv 0.83 0.85 2
rs7396187
DKK3
0.925 0.120 11 11967604 intron variant C/G snv 0.84 2