Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs756522395
ATM
1.000 0.080 11 108257484 missense variant C/G;T snv 1
rs28904921
C11orf65 ; ATM
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 6
rs566164
CCDC162P
1.000 0.080 6 109185258 intron variant A/G snv 0.73 1
rs753904217
GSTM2 ; GSTM1
1.000 0.080 1 109690557 missense variant G/A snv 1.9E-04 6.6E-05 1
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 26
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 3
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 16
rs2420946
FGFR2
0.851 0.160 10 121591810 intron variant T/C snv 0.56 4
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 20
rs4645959
CASC11 ; MYC
0.882 0.080 8 127738294 missense variant A/C;G snv 1.6E-05; 2.3E-02 3
rs28359178
CYTB ; ND5 ; ND6
0.882 0.280 MT 13708 missense variant G/A snv 2
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
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 17
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs3218536
XRCC2
0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs143282828
UIMC1
1.000 0.080 5 176968697 missense variant A/G snv 7.3E-04 7.3E-04 1
rs203462
AKAP10
0.807 0.200 17 19909228 missense variant T/C snv 0.37 0.43 6
rs796096871
AKAP10
0.807 0.200 17 19909228 missense variant TG/CA mnv 6
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs13010627
CASP10
0.807 0.280 2 201209375 missense variant G/A snv 4.2E-02 4.3E-02 10
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs28997576
BARD1
0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs2070094
BARD1
0.882 0.080 2 214767531 missense variant C/A;T snv 1.6E-05; 0.37 3
rs386654966
BARD1
0.882 0.080 2 214767531 missense variant CA/AG;TG mnv 3