Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 17
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 7
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 7
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 6
rs35850753
TP53
0.807 0.080 17 7675353 5 prime UTR variant C/T snv 1.3E-02 6
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 4
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 4
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 4
rs59060240
EGFR
0.882 0.040 7 55080369 intron variant AA/-;A;AAA;AAAA;AAAAAAAAAAA delins 4
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs3851634
POLR3B
0.882 0.040 12 106419124 intron variant T/C snv 0.22 4
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs2562152
RHBDF1
0.882 0.040 16 73898 intron variant A/T snv 0.67 4
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 4
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 4
rs2235573
SLC16A8
0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4