Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867114783
TP53
17 7675109 missense variant T/C snv 6
rs104894194
AIP
0.925 11 67483198 stop gained C/T snv 2.8E-05 2.1E-05 4
rs140516819
EGFR
7 55172999 missense variant A/C;G snv 4.0E-05 2.4E-04 4
rs1441008398
APC
5 112839334 missense variant C/T snv 4.0E-06 4
rs35918369
EGFR
7 55205613 missense variant C/T snv 3.1E-04 3.3E-04 4
rs397507828
BRCA2
1.000 13 32340440 stop gained G/T snv 4
rs397508838
BRCA1
0.925 17 43094416 stop gained C/T snv 7.0E-06 4
rs750605522
GOT2
16 58722168 missense variant T/A snv 4.0E-06 7.0E-06 4
rs767136747
SARDH
9 133717404 missense variant T/C snv 4.0E-06 4
rs876660427
APC
5 112838608 missense variant C/T snv 4
rs121913381
CDKN2A
9 21971037 missense variant C/A;T snv 3
rs151227402
SLC2A9 ; DRD5
4 9783126 missense variant A/G snv 8.0E-05 3.1E-04 3
rs16861205
ADIPOQ
3 186843845 intron variant G/A snv 0.14 3
rs200397144
SDHA
1.000 5 251427 missense variant C/G;T snv 2.4E-05; 4.0E-06 3
rs2071214
BIRC5
17 78223510 missense variant G/A snv 0.93 0.96 3
rs371217738
ADRA2B
2 96115056 missense variant C/A;T snv 8.1E-06 3
rs375526265
APEX1
14 20457260 missense variant C/T snv 1.2E-05 2.8E-05 3
rs4940177
DCC
18 52342374 intron variant T/C;G snv 3
rs556324078
EGFR
7 55205514 missense variant T/C snv 4.0E-06 3
rs750600586
TP53
17 7675199 missense variant G/A;T snv 3
rs761546875
MDM2
12 68816914 missense variant G/C snv 4.0E-06 3
rs767543501
MUL1
1 20502133 missense variant C/A;G snv 4.0E-06; 1.6E-05 3
rs771246666
DRD5 ; SLC2A9
4 9783122 frameshift variant T/- delins 4.4E-05 3
rs772173802
DACT3-AS1 ; PRKD2
0.925 19 46674559 missense variant G/T snv 4.0E-06 3
rs864622017
E2F1
20 33679830 missense variant C/T snv 3