Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs4932158
IDH2-DT
1.000 0.080 15 90106171 intron variant A/G;T snv 1
rs11540478
IDH2
0.851 0.080 15 90085305 synonymous variant G/A;C snv 3.5E-02; 6.4E-06 4
rs13312840
NBN
0.882 0.120 8 89985681 intron variant A/G;T snv 3
rs778998026
NBN
0.925 0.200 8 89981502 missense variant C/G;T snv 1.6E-05 2
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs779346343
NBN
0.925 0.200 8 89970379 missense variant A/G snv 4.0E-06 7.0E-06 2
rs746965070
NBN
0.827 0.200 8 89955487 missense variant T/C snv 1.2E-05 5
rs1060503460
NBN
0.925 0.200 8 89955461 missense variant A/T snv 2
rs1061302
NBN
0.827 0.160 8 89946194 synonymous variant T/C snv 0.35 0.30 5
rs8252
GADD45G ; LOC105376139
1.000 0.080 9 89606095 3 prime UTR variant C/T snv 4.5E-02 4.9E-02 1
rs2279574
DUSP6
0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 8
rs373572
RAD18
0.882 0.120 3 8913705 missense variant C/T snv 0.68 0.70 6
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 5
rs4148149
ABCG2
1.000 0.080 4 88141133 intron variant T/G snv 0.42 1
rs2231137
ABCG2
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 13
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2725264
ABCG2
1.000 0.080 4 88104957 intron variant C/T snv 0.70 1
rs4754
SPP1
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 25
rs57374291
PTEN
1.000 0.080 10 87933078 missense variant G/A;T snv 2
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs979090956
ABCB1
0.827 0.200 7 87553822 missense variant G/C snv 5
rs201661522
ABCB1
1.000 0.080 7 87539293 missense variant A/G snv 6.4E-05 1.0E-04 2