Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1458511470
CASP8
2 201272639 frameshift variant -/C delins 2
rs17524488
SPP1
0.925 0.040 4 87975555 non coding transcript exon variant -/G delins 4
rs11267092
F2R
5 76715788 intron variant -/GGCCGCGGGAAGC;GGCCGCGGGAAGCGGCCGCGGGAAGC delins 2
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs866419664
TP53
0.882 0.040 17 7673821 frameshift variant -/TCCCA delins 5
rs3830675
PTEN
1.000 0.040 10 87931195 intron variant -/TCTTA delins 3
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs17880560
TP53
17 7668169 intron variant -/TGGCCG delins 2
rs71305152
ZFPM2
0.882 0.040 8 105437494 intron variant -/TTTTCT delins 0.43 5
rs397509239
BRCA1
1.000 17 43057122 frameshift variant A/- del 3
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs2239704
LTA ; LOC100287329
0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 17
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs735482
CD3EAP ; ERCC1
0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs7763881
HULC ; LOC100506207
0.776 0.160 6 8653014 non coding transcript exon variant A/C snv 0.44 11
rs1204382931
CYP1B1 ; CYP1B1-AS1
0.790 0.160 2 38075270 missense variant A/C snv 4.3E-06 10
rs1566734
PTPRJ
0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 10
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs627928
RNASEL
0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10
rs2410373 0.851 0.120 8 16066997 intergenic variant A/C snv 0.34 6