Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555876140
SMARCB1
22 23793671 frameshift variant -/C delins 1
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs11706832
LRIG1
1.000 0.040 3 66452557 intron variant A/C;G snv 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs10494090
SLC25A24
1.000 0.040 1 108150714 intron variant A/C;G;T snv 2
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs11163687
LOC107985037
1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs12723208
TRAF5
1.000 0.040 1 211337552 intron variant A/G snv 0.13 2
rs7572263
C2orf80
1.000 0.040 2 208186862 intron variant A/G snv 0.27 2
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 10
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs648044
ZBTB16 ; LOC101928875
0.882 0.040 11 114160077 non coding transcript exon variant A/G;T snv 4
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs2562152
RHBDF1
0.882 0.040 16 73898 intron variant A/T snv 0.67 4
rs59060240
EGFR
0.882 0.040 7 55080369 intron variant AA/-;A;AAA;AAAA;AAAAAAAAAAA delins 4
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs11598018
STN1
1.000 0.040 10 103901557 intron variant C/A;T snv 2
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs35850753
TP53
0.807 0.080 17 7675353 5 prime UTR variant C/T snv 1.3E-02 8