Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104893624
LOC112268426 ; CXCR4
0.851 0.200 2 136114928 stop gained G/A snv 4
rs1050274678
SLC19A1
0.925 0.040 21 45530803 missense variant C/T snv 1.1E-05 7.0E-06 3
rs1057910
CYP2C9
0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs10824095
ADK
0.925 0.040 10 74176853 5 prime UTR variant C/G;T snv 0.67 2
rs11141915
DAPK1
0.882 0.160 9 87620879 intron variant A/C snv 0.25 3
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs11706052
IMPDH2
0.882 0.080 3 49026677 intron variant A/G snv 8.3E-02 7.6E-02 3
rs11719165 0.925 0.040 3 194865359 intergenic variant T/C snv 0.53 2
rs12046844 0.925 0.040 1 65772696 regulatory region variant G/A snv 0.17 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1260186456
ABCC1
0.925 0.040 16 16102659 missense variant G/T snv 9.4E-06 2
rs12720066
ABCB1
0.925 0.040 7 87540386 intron variant A/C snv 3.9E-02 2
rs12934241
MMP2
0.925 0.040 16 55486666 non coding transcript exon variant C/G;T snv 2
rs1326123837
SLC37A4 ; TRAPPC4
0.925 0.040 11 119025310 missense variant C/T snv 7.0E-06 2
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1422359334
GSTK1 ; LOC105375545
0.925 0.040 7 143264131 missense variant C/A;T snv 4.0E-06 2
rs1424665740
SLC10A2
0.925 0.040 13 103066068 missense variant T/C snv 4.0E-06 7.0E-06 2