Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs5751129
XRCC6 ; DESI1
0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs132774
XRCC6
0.776 0.280 22 41635949 intron variant C/G snv 0.69 9
rs8190315
BID
0.851 0.240 22 17743998 missense variant T/C snv 2.4E-02 3.6E-02 5
rs9862
TIMP3 ; SYN3
1.000 0.080 22 32857293 missense variant T/A;C snv 4.0E-06; 0.55 3
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs1237063529
CBS
0.752 0.360 21 43058894 missense variant T/G snv 5.6E-06 13
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs2296241
CYP24A1
0.763 0.200 20 54169680 synonymous variant G/A snv 0.49 0.51 12
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 7
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
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 11
rs1406
CCNE1
0.882 0.120 19 29824205 3 prime UTR variant C/A snv 0.28 4
rs281377
FUT2 ; LOC105447645
0.925 0.120 19 48703346 synonymous variant C/T snv 0.49 0.42 4
rs33438
ZNF536
1.000 0.080 19 30454165 intron variant G/A snv 0.50 2
rs2289520
SERPINB5
0.925 0.120 18 63493087 missense variant G/A;C snv 0.14 3
rs1373756 1.000 0.120 18 52259936 intergenic variant C/T snv 0.24 2