Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 16
rs11655505
NBR2 ; BRCA1
0.776 0.160 17 43126360 intron variant G/A snv 0.31 8
rs3212964
ERCC1
0.851 0.120 19 45417538 intron variant C/T snv 0.18 4
rs2987983
ESR2
0.882 0.080 14 64296935 intron variant A/G snv 0.40 3
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 17
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
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 0.30 103
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
rs3218536
XRCC2
0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs368087026
SLC19A1
0.637 0.520 21 45530890 missense variant G/A snv 33
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 19
rs3741378
SIPA1
0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 5
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
rs182176585
NAA16
1.000 0.080 13 41372227 missense variant G/A;C snv 1.3E-04; 4.3E-06 1
rs373204088
SLC38A1
1.000 0.080 12 46209126 missense variant C/T snv 4.1E-06 7.0E-06 1
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