Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3212964
ERCC1
0.851 0.120 19 45417538 intron variant C/T snv 0.18 4
rs3218536
XRCC2
0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs34301344
ARL11
0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs368087026
SLC19A1
0.637 0.520 21 45530890 missense variant G/A snv 33
rs373204088
SLC38A1
1.000 0.080 12 46209126 missense variant C/T snv 4.1E-06 7.0E-06 1
rs3741378
SIPA1
0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 8
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986938
ESR2
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs587782555
BARD1
0.882 0.080 2 214728935 missense variant A/G snv 7.0E-06 3
rs730881500
BRCA1
0.882 0.080 17 43045769 missense variant G/A snv 8.0E-06 3
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7350
H2AX
1.000 0.080 11 119094338 3 prime UTR variant G/A snv 0.30 1
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs775144154
SLC19A1
0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs7759
DPAGT1 ; H2AX
0.882 0.080 11 119096581 3 prime UTR variant A/G snv 0.30 3
rs80356892
BRCA1
1.000 0.080 17 43092965 missense variant A/G snv 1.7E-03 4.5E-04 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
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
rs968728714
VDR
1.000 0.080 12 47904629 start lost A/G;T snv 1.5E-05; 7.4E-06 1