Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs8057643
RBFOX1
0.851 0.040 16 6910689 intron variant C/A;T snv 4
rs10464870
CCDC26
0.882 0.040 8 129465577 intron variant C/T snv 0.80 3
rs12645561
NEIL3
0.882 0.120 4 177339718 intron variant C/A;T snv 3
rs145929329
CDKN2B-AS1
0.882 0.040 9 22066213 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT delins 0.58 3
rs2033214
RBBP6
0.882 0.040 16 24566199 intron variant T/G snv 0.14 3
rs6470745
CCDC26
0.882 0.040 8 129629675 intron variant A/G snv 0.18 3
rs2291427
ALOX5
0.925 0.040 10 45440776 intron variant A/G;T snv 2
rs7325927
FAM155A-IT1 ; FAM155A
0.925 0.040 13 107823165 intron variant C/T snv 0.38 2
rs7732320
SSBP2
0.925 0.040 5 81423306 intron variant C/T snv 0.22 2
rs9642393
EGFR
0.925 0.040 7 55177954 intron variant T/C snv 0.24 2
rs144551722 0.851 0.040 X 43632629 intergenic variant G/A snv 0.13 4
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs13332653 0.882 0.040 16 24578078 intergenic variant T/G snv 0.11 3
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs863225401
MSH6 ; FBXO11
0.925 0.040 2 47799866 stop gained G/A snv 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213