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
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
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800372
TP53
0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs1056892
CBR3-AS1 ; CBR3
0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39 6
rs7853758
LOC105376116 ; SLC28A3
0.851 0.120 9 84286011 synonymous variant G/A snv 0.15 0.19 5
rs17863783
UGT1A6 ; UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A8
0.827 0.200 2 233693631 synonymous variant G/T snv 3.8E-02 5.5E-02 5
rs1805389
LIG4
0.882 0.080 13 108211261 missense variant G/A;C;T snv 5.7E-02; 4.1E-06 4
rs4342822
LOC105372912 ; PROX1-AS1
0.882 0.080 1 213850882 intron variant G/T snv 0.62 3
rs2229774
RARG
0.882 0.280 12 53211761 missense variant G/A snv 7.3E-02 7.3E-02 3
rs114971217 0.925 0.080 2 236525150 intergenic variant T/A;C snv 2
rs11651604 0.925 0.080 17 71440368 regulatory region variant G/A;C snv 2
rs140236920 0.925 0.120 5 18186317 intergenic variant -/TAAAT delins 2
rs147512482 0.925 0.080 22 27215781 intergenic variant C/G snv 2.4E-03 2
rs1519277 0.925 0.080 2 123261223 intergenic variant C/T snv 0.12 2
rs35669975 0.925 0.120 13 107138053 intergenic variant C/A;G snv 2
rs4971486 0.925 0.120 2 4847728 regulatory region variant C/G snv 0.23 2
rs7333181 1.000 0.040 13 111568950 intergenic variant G/A snv 0.11 2
rs12646911
GLRA3
0.925 0.120 4 174701439 intron variant G/A snv 0.75 2