Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs368087026
SLC19A1
0.637 0.520 21 45530890 missense variant G/A snv 33
rs34301344
ARL11
0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs2228480
ESR1
0.724 0.360 6 152098960 synonymous variant G/A snv 0.19 0.18 16
rs11655505
NBR2 ; BRCA1
0.776 0.160 17 43126360 intron variant G/A snv 0.31 8
rs2233682
PIN1
0.827 0.240 19 9838476 synonymous variant G/A snv 3.7E-02 6.3E-02 5
rs730881500
BRCA1
0.882 0.080 17 43045769 missense variant G/A snv 8.0E-06 3
rs7350
H2AX
1.000 0.080 11 119094338 3 prime UTR variant G/A snv 0.30 1
rs2233678
PIN1 ; LOC100996288
0.732 0.360 19 9834503 non coding transcript exon variant G/A;C snv 14
rs1351211430
ERCC2
0.851 0.120 19 45369118 synonymous variant G/A;C snv 8.0E-06 4
rs182176585
NAA16
1.000 0.080 13 41372227 missense variant G/A;C snv 1.3E-04; 4.3E-06 1
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2272125
FANCD2 ; FANCD2OS
1.000 0.080 3 10096385 synonymous variant T/G snv 0.18 0.25 1