Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7246045
CGB5
0.882 0.120 19 49042825 upstream gene variant T/G snv 2.9E-02 5
rs11084033
LOC105372441
0.882 0.120 19 50850699 intron variant C/A;T snv 4
rs121913322
STK11
0.882 0.120 19 1221320 missense variant C/A;G;T snv 2.9E-05; 1.2E-04 4
rs266851
KLK15 ; LOC105372441
0.882 0.120 19 50833083 intron variant C/T snv 0.20 3
rs34529039
CEBPA ; CEBPA-DT
0.882 0.120 19 33301725 synonymous variant C/A snv 0.19 0.16 3
rs7260002
CGB5
0.882 0.120 19 49042615 non coding transcript exon variant A/C;G snv 0.46 3
rs759920
DNMT1
0.882 0.120 19 10174102 intron variant A/G;T snv 3
rs12373237
LAMA3
0.851 0.200 18 23845972 intron variant G/A snv 0.47 5
rs495139
ENOSF1
0.882 0.120 18 676008 intron variant G/C snv 0.63 4
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26
rs138213197
HOXB13
0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs2240308
AXIN2
0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs28897672
BRCA1
0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 16
rs137852986
BRIP1
0.732 0.440 17 61716051 stop gained G/A snv 1.7E-04 1.5E-04 13
rs1799950
BRCA1
0.752 0.240 17 43094464 missense variant T/C snv 4.7E-02 4.6E-02 13
rs3760396
CCL2
0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15 13
rs41293459
BRCA1
0.763 0.280 17 43063930 missense variant C/A;G;T snv 2.4E-05 12