Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1558518449
MSH2
1.000 0.040 2 47475221 frameshift variant ATGACGTA/- delins 1
rs2291427
ALOX5
0.925 0.040 10 45440776 intron variant A/G;T snv 2
rs1555138291
ATM ; C11orf65
0.925 0.240 11 108345859 stop gained G/A snv 2
rs11548193
BCAT2
0.925 0.040 19 48799813 missense variant G/A;C snv 0.14 2
rs11670188
BTBD2
0.925 0.040 19 2014038 non coding transcript exon variant A/G snv 0.16 2
rs1558650888
DNMT3A
0.925 0.040 2 25234308 missense variant G/A snv 2
rs9642393
EGFR
0.925 0.040 7 55177954 intron variant T/C snv 0.24 2
rs7325927
FAM155A-IT1 ; FAM155A
0.925 0.040 13 107823165 intron variant C/T snv 0.38 2
rs3829382
FLT3
0.925 0.040 13 28003551 3 prime UTR variant G/T snv 0.46 2
rs11558961
GFAP
0.925 0.040 17 44907319 3 prime UTR variant G/C;T snv 0.27; 1.2E-05 2
rs759927375
H4C1 ; H3C1
0.925 0.040 6 26020589 missense variant G/A;C snv 1.2E-05; 8.0E-06 2
rs1435266782
IDH2
0.925 0.040 15 90088633 missense variant C/A;T snv 4.0E-06 2
rs751859698
MSH4
0.925 0.040 1 75898031 missense variant T/A;C snv 1.2E-05 2
rs587782603
PTEN
1.000 0.040 10 87952118 stop gained G/A;T snv 2
rs8957
SLC2A4RG
0.925 0.040 20 63742354 missense variant G/T snv 0.71 0.78 2
rs7732320
SSBP2
0.925 0.040 5 81423306 intron variant C/T snv 0.22 2
rs13332653 0.882 0.040 16 24578078 intergenic variant T/G snv 0.11 3
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs10464870
CCDC26
0.882 0.040 8 129465577 intron variant C/T snv 0.80 3
rs6470745
CCDC26
0.882 0.040 8 129629675 intron variant A/G snv 0.18 3
rs145929329
CDKN2B-AS1
0.882 0.040 9 22066213 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT delins 0.58 3
rs1346787
EFEMP1 ; LOC112268416
0.882 0.040 2 55865477 downstream gene variant C/A;G;T snv 3
rs1057519887
EGFR
0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs1057519888
EGFR
0.925 0.080 7 55143386 missense variant A/G snv 3
rs139236063
EGFR
0.925 0.080 7 55165350 missense variant G/C;T snv 3