Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs799917
BRCA1
0.708 0.320 17 43092919 missense variant G/A;C;T snv 0.40; 1.6E-05 18
rs13706
CDC6
0.776 0.200 17 40300899 missense variant G/A;C snv 0.15; 8.0E-06 11
rs16941
BRCA1
0.827 0.240 17 43092418 missense variant T/C;G snv 0.35 7
rs1335035506
SHMT1
1.000 0.120 17 18340207 missense variant A/G snv 4.0E-06 1.4E-05 1
rs148701087
SHMT1 ; MIR6778
1.000 0.120 17 18340762 missense variant G/A snv 6.4E-04 8.8E-04 1
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs441399 1.000 0.120 15 90822992 regulatory region variant G/A snv 0.50 1
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs1053667
TOGARAM1
0.925 0.120 14 45073835 3 prime UTR variant T/C snv 0.11 4
rs4901706
TMEM260
1.000 0.120 14 56647667 3 prime UTR variant G/A;C;T snv 3
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs2582869
TNFSF13B
1.000 0.120 13 108259797 intron variant A/G;T snv 1
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs16917496
KMT5A
0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs2682818
MIR618 ; LOC105369869 ; LIN7A
0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs4516035
VDR
0.776 0.360 12 47906043 non coding transcript exon variant T/C snv 0.31 10
rs3660
KRT86 ; KRT81
0.882 0.160 12 52286153 3 prime UTR variant C/G snv 0.51 6