Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730882002
TP53
0.925 0.040 17 7674956 missense variant T/C snv 6
rs10248565
HDAC9
1.000 0.040 7 18935100 intron variant T/G snv 0.14 3
rs767505234
EGFR
1.000 0.040 7 55174033 missense variant C/T snv 1.4E-05 3
rs977818812
ERBB2
1.000 0.040 17 39723608 missense variant A/T snv 3
rs1057519731
MAP2K1
0.925 0.040 15 66436816 missense variant G/C snv 2
rs1057519785
ALK
1.000 0.040 2 29222404 missense variant A/C snv 2
rs1057519787
ERBB2
1.000 0.040 17 39711952 missense variant G/A;C snv 2
rs1057519856
MAP2K1
0.925 0.040 15 66436815 missense variant T/A snv 2
rs1131692237
ERBB2 ; MIR4728
1.000 0.040 17 39725161 missense variant T/G snv 2
rs1131692238
CDK12
0.925 0.040 17 39509731 missense variant G/T snv 2
rs1315148641
APOBEC1
1.000 0.040 12 7654617 missense variant T/C snv 4.0E-06 2
rs1356083197
CNIH3 ; WDR26
1.000 0.040 1 224434068 missense variant C/T snv 1.5E-05 1.4E-05 2
rs1431090090
ZEB1
1.000 0.040 10 31520347 missense variant C/A snv 4.0E-06 2
rs1464381306
PECAM1
1.000 0.040 17 64390632 missense variant A/T snv 1.4E-05 2
rs16970006
LOC112268142 ; CHRNB4
1.000 0.040 15 78677917 intron variant T/C snv 8.7E-02 2
rs200298588
PDLIM5
1.000 0.040 4 94575722 missense variant G/A snv 2
rs2004038
ADAMTS7
1.000 0.040 15 78779064 intron variant G/A snv 0.33 2
rs2608029
PVT1
1.000 0.040 8 128157880 intron variant C/G snv 0.37 2
rs3885951
HYKK
1.000 0.040 15 78533575 missense variant A/G snv 7.5E-02 6.9E-02 2
rs4947492
EGFR
0.925 0.040 7 55120299 intron variant G/A snv 0.50 2
rs746540053
CD34 ; LOC107985253
1.000 0.040 1 207911034 missense variant C/T snv 2
rs754284524
SRFBP1 ; LOX
1.000 0.040 5 122074125 stop gained -/TACATGCTAGATTCATTTTAACTCAATACTGCCATTCAATTCTAGCAAC ins 4.0E-06 2
rs759404153
EPHB2
1.000 0.040 1 22910452 missense variant T/A;G snv 2.8E-05; 4.0E-06 2
rs78442819
TEKT5
1.000 0.040 16 10647125 intron variant G/C snv 0.13 2
rs896171398
ERBB2
1.000 0.040 17 39709846 missense variant G/A;C snv 1.6E-05 2