Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1264171723
LOC112268270 ; BMP7
1.000 0.040 20 57266050 missense variant G/A snv 7.0E-06 1
rs17305657
BPIFA3
1.000 0.040 20 33218782 intron variant T/C snv 5.2E-02 1
rs6058339
PHF20
1.000 0.040 20 35872557 intron variant C/T snv 0.94 1
rs721970 1.000 0.040 20 33315727 upstream gene variant A/G snv 0.96 1
rs7271289
NCOA6
1.000 0.040 20 34809500 5 prime UTR variant C/T snv 0.15 1
rs773962041
SSTR4
1.000 0.040 20 23036363 missense variant C/G snv 1.6E-05 1
rs910871
NCOA6
1.000 0.040 20 34745404 intron variant C/A snv 0.85 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 12
rs1057519742
GNA11
0.827 0.160 19 3118944 missense variant A/C;T snv 7
rs121913315
STK11
0.882 0.160 19 1220488 missense variant G/A;T snv 5
rs1024708183
MAP2K7
0.925 0.040 19 7909761 missense variant A/G snv 4
rs1057519806
MAP2K2
0.882 0.200 19 4110583 missense variant T/C snv 3
rs1057519808
MAP2K2
1.000 0.040 19 4117543 missense variant T/G snv 2
rs121913323
STK11
1.000 0.040 19 1220416 stop gained C/T snv 2
rs137853080
STK11
1.000 0.040 19 1207058 missense variant T/G snv 2
rs137853081
STK11
1.000 0.040 19 1219352 missense variant G/C;T snv 2
rs1057519807
MAP2K2
1.000 0.040 19 4110586 missense variant A/T snv 1
rs1057519809
MAP2K2
1.000 0.040 19 4117586 missense variant G/A;C snv 4.0E-06 1
rs1057519810
MAP2K2
1.000 0.040 19 4117619 missense variant C/A;T snv 4.0E-06 1