Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10009228
CHRNA9
4 40354405 missense variant A/G snv 0.78 0.76 1
rs2073778
DGCR8
22 20087052 non coding transcript exon variant C/T snv 0.12 1
rs720012
DGCR8
22 20111059 3 prime UTR variant G/A snv 0.12 1
rs1057519771
ABL1
1.000 0.080 9 130872201 missense variant G/C snv 2
rs762807774
SDF4
1.000 0.040 1 1228495 frameshift variant CGCGGCTCCGC/-;CGCGGCTCCGCCGCGGCTCCGC delins 7.0E-06 2
rs587782148
TP53
17 7676113 missense variant C/T snv 2
rs961150162
EGFR
7 55198779 missense variant G/A;C snv 3
rs557263543
FGFR1
8 38412508 3 prime UTR variant C/T snv 3
rs55958994
KRT8
0.925 0.080 12 52907235 intron variant C/T snv 0.12 3
rs11672691
PCAT19
0.925 0.080 19 41479679 non coding transcript exon variant G/A snv 0.42 3
rs969139366
PDGFRA
4 54277974 missense variant T/C snv 3.5E-05 3
rs438034
CENPF
0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4
rs201216664
NME1-NME2 ; NME2
0.851 0.080 17 51171503 missense variant A/G snv 5
rs1288373809
TP53
0.882 0.120 17 7673255 synonymous variant G/A snv 5.3E-06 5
rs200863613
CDKN2A
0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs7121
GNAS
0.882 0.160 20 58903752 missense variant C/G;T snv 0.54 6
rs773862672
MTOR
0.882 0.280 1 11247922 missense variant G/A;C snv 1.2E-05 6
rs1443465532
VEGFA
0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs587782529
TP53
0.851 0.200 17 7670700 missense variant G/A;C snv 8
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs2016347
IGF1R
0.790 0.160 15 98960571 3 prime UTR variant G/A;T snv 9
rs767808984
NKX2-1-AS1 ; SFTA3 ; NKX2-1
0.851 0.160 14 36520098 missense variant C/G;T snv 1.3E-05 9
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs367597251
MDM2
0.807 0.080 12 68839587 missense variant A/G snv 1.5E-04 5.1E-04 10
rs17217772
MSH2
0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 10