Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28357681
ND6 ; CYTB
0.851 0.040 MT 14798 missense variant T/C snv 4
rs144551722 0.851 0.040 X 43632629 intergenic variant G/A snv 0.13 4
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs2904551
PRODH
0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 8
rs2017309
CHEK2
0.851 0.040 22 28735438 intron variant T/A snv 0.23 4
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs3788266
S100B
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 10
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs55819519
TP53
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs371409680
TP53
0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9