Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs3124599
NOTCH1
0.851 0.080 9 136509318 intron variant G/A snv 0.13 5
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs6790167
TP63
0.827 0.080 3 189869485 intron variant A/G snv 0.53 5
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 4
rs439680 1.000 0.080 5 109998341 regulatory region variant C/G snv 3
rs55985569
MET
0.925 0.080 7 116699588 missense variant G/A;T snv 3.7E-03 3
rs1360583020
PXN
1.000 0.080 12 120215202 missense variant G/C snv 4.3E-06 2
rs397517097
EGFR
0.851 0.080 7 55174777 missense variant T/C snv 2
rs942190
TDP1 ; EFCAB11
1.000 0.080 14 89956320 intron variant T/C snv 0.37 2
rs12666409
DDC
1.000 0.080 7 50567279 upstream gene variant T/A snv 0.21 1
rs1778335
PIP4K2A
1.000 0.080 10 22643219 intron variant T/C snv 0.27 1
rs312599 1.000 0.080 5 143998425 intergenic variant C/T snv 0.33 1
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 1
rs55853698
CHRNA5
0.882 0.080 15 78565597 5 prime UTR variant T/G snv 0.25 1
rs587781495
TP53
1.000 0.080 17 7676005 missense variant C/T snv 1
rs7519667
WDR64
1.000 0.080 1 241722005 intron variant C/T snv 0.78 1
rs775800262
EGFR
1.000 0.080 7 55155894 missense variant G/T snv 4.0E-06 1
rs1045494
CASP8
0.882 0.120 2 201287058 3 prime UTR variant T/C snv 0.10 3
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 17
rs1799814
CYP1A1
0.807 0.160 15 74720646 missense variant G/A;T snv 1.6E-05; 3.1E-02 8
rs577715207
TP63
0.827 0.160 3 189886413 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 8
rs34589476
MET
0.827 0.160 7 116771869 missense variant C/T snv 2.9E-03 3.2E-03 7
rs4353229
CASP7
0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6