Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9293329
XRCC4
0.882 0.080 5 83100768 intron variant G/A snv 7.3E-02 3
rs928508
NFYC ; MIR30C1
0.851 0.080 1 40757742 intron variant G/A;T snv 0.50 4
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs9280508
TRIM27
0.882 0.080 6 28914582 intron variant GG/-;G;GGG;GGGG;GGGGG;GGGGGG delins 3
rs926198
CAV1
0.851 0.120 7 116527154 intron variant C/A;T snv 4
rs9261204
ZNRD1ASP
0.790 0.200 6 30037466 intron variant A/G snv 0.17 9
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
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
rs887468
POU5F1 ; PSORS1C3
0.882 0.080 6 31173746 non coding transcript exon variant C/T snv 0.26 3
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 1
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 23
rs884225
EGFR
0.827 0.160 7 55206391 3 prime UTR variant T/C;G snv 5
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876659871
CHEK2
0.882 0.080 22 28719462 missense variant C/T snv 7.0E-06 3
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 24
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs868188
ARHGEF11 ; MIR765 ; LRRC71
0.882 0.080 1 156937323 missense variant T/C snv 0.40 0.33 3
rs868021367
BRAF
0.882 0.080 7 140753319 missense variant C/G snv 3
rs863582
MUC4
0.882 0.080 3 195751823 non coding transcript exon variant G/A snv 0.59 3
rs863224682
TP53
1.000 0.080 17 7669655 missense variant C/A;T snv 4.0E-06 2
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs859769
MUC4
0.882 0.080 3 195807542 intron variant G/T snv 0.54 3
rs859
STARD5 ; IL16
0.807 0.200 15 81308981 3 prime UTR variant A/G snv 0.33 6
rs851797
EXO1
0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10