Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs20575
TNFRSF10A
0.645 0.440 8 23201811 missense variant C/G snv 0.54 0.44 29
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs13254990
PVT1
0.882 0.120 8 128064205 intron variant C/T snv 0.24 4
rs1493202
XKR9
1.000 0.120 8 70993352 intron variant T/G snv 0.41 1
rs1805329
RAD23B
0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 15
rs12917
MGMT ; LOC105378560
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2308321
MGMT
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs2308327
MGMT
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02 10
rs12355840
MIR202 ; MIR202HG
0.827 0.240 10 133247608 non coding transcript exon variant C/G;T snv 1.1E-04; 0.80 5
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 8
rs4937362
LOC105369568
0.827 0.240 11 128622844 intron variant T/C snv 0.49 5
rs4938573 0.851 0.280 11 118871133 regulatory region variant C/T snv 0.79 4
rs1159838942
RAG1
1.000 0.120 11 36574757 missense variant C/A;T snv 1
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs2682818
MIR618 ; LOC105369869 ; LIN7A
0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs4760655
VDR
1.000 0.120 12 47900348 intron variant G/A snv 0.72 1
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2228479
MC1R
0.763 0.280 16 89919532 missense variant G/A;C snv 7.8E-02; 4.0E-06 11
rs587781386
TP53
0.882 0.120 17 7674889 missense variant A/C;G snv 3.2E-05; 4.0E-06 3