Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs3024994
VEGFA
0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs1453633223
CDKN2A
0.807 0.080 9 21974503 missense variant C/T snv 4.0E-06 6
rs1340827343
TCF19 ; POU5F1
0.851 0.040 6 31165259 missense variant C/T snv 4
rs1381537616
HOXA10 ; HOXA9 ; HOXA10-HOXA9
0.851 0.040 7 27174132 missense variant C/T snv 4
rs200187877
PPARGC1A
0.851 0.040 4 23795829 missense variant C/T snv 8.0E-06 7.0E-06 4
rs375391381
FRMD5
0.851 0.040 15 43883735 missense variant C/T snv 8.0E-06 1.4E-05 4
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1800734
EPM2AIP1 ; MLH1
0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 25
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs11554137
IDH1
0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs3788266
S100B
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs769809364
TP73
0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7
rs373584770
CASP1
0.827 0.120 11 105030337 missense variant G/A snv 4.0E-06 7.0E-06 5
rs771563543
ZEB1
0.851 0.040 10 31510841 missense variant G/A snv 4.0E-06 1.4E-05 5
rs1029044314
DDR1
0.851 0.040 6 30898095 missense variant G/A snv 4
rs144551722 0.851 0.040 X 43632629 intergenic variant G/A snv 0.13 4
rs1957106
NFKBIA
0.851 0.040 14 35404564 synonymous variant G/A snv 0.28 0.25 4
rs766265850
MIR4640 ; DDR1
0.851 0.040 6 30889239 missense variant G/A snv 8.1E-06 7.0E-06 4
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44