Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs34301344
ARL11
0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
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
rs7759
DPAGT1 ; H2AX
0.882 0.080 11 119096581 3 prime UTR variant A/G snv 0.30 3
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs3212964
ERCC1
0.851 0.120 19 45417538 intron variant C/T snv 0.18 4
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs1351211430
ERCC2
0.851 0.120 19 45369118 synonymous variant G/A;C snv 8.0E-06 4
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs2228480
ESR1
0.724 0.360 6 152098960 synonymous variant G/A snv 0.19 0.18 16
rs4986938
ESR2
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs2987983
ESR2
0.882 0.080 14 64296935 intron variant A/G snv 0.40 3
rs2272125
FANCD2 ; FANCD2OS
1.000 0.080 3 10096385 synonymous variant T/G snv 0.18 0.25 1
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 16
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs7350
H2AX
1.000 0.080 11 119094338 3 prime UTR variant G/A snv 0.30 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
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
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
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
rs182176585
NAA16
1.000 0.080 13 41372227 missense variant G/A;C snv 1.3E-04; 4.3E-06 1
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