Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 25
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 23
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 17
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 16
rs7003908
PRKDC
0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs1801320
RAD51 ; RAD51-AS1
0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv 14
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs11554137
IDH1
0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs4652
LGALS3
0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs3788266
S100B
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12