Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs60745952
LOC107986195 ; LOC105377481
0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs6973569
NPSR1-AS1
0.851 0.080 7 34583412 intron variant G/A snv 4.7E-02 5
rs8103851
PRKCG
0.851 0.040 19 53894400 intron variant C/G snv 0.44 5
rs11016879
MGMT
0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs2064863
AURKA
0.925 0.120 20 56387716 intron variant T/A;C;G snv 4
rs2835931
KCNJ6
1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 4
rs477145
TIAM1
1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs6464926
EZH2
0.882 0.120 7 148821919 intron variant C/T snv 0.41 4
rs7034162
NFIB
0.882 0.040 9 14190288 intron variant A/T snv 0.81 4
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs7668666
TLR3
1.000 4 186080138 intron variant C/A;T snv 4
rs1040411
ATG5
1.000 0.120 6 106150148 intron variant G/A snv 0.47 3
rs11121704
MTOR
1 11233902 intron variant C/A;T snv 3
rs3756824
PRL ; CASC15
0.925 0.080 6 22298508 intron variant C/G;T snv 3
rs4946728
ATG5
1.000 0.120 6 106142488 intron variant A/C snv 0.72 3
rs6983561
PCAT1 ; CASC19
0.925 0.080 8 127094635 intron variant A/C snv 0.17 3
rs7371084
GTF2A1L ; LHCGR ; STON1-GTF2A1L
0.925 0.120 2 48712814 intron variant T/C snv 0.12 3
rs1347591
NUP93
1.000 0.080 16 56834788 intron variant A/G snv 0.47 0.47 2
rs2286742
HABP2
1.000 0.080 10 113580733 intron variant G/A;C snv 0.57; 8.2E-06 2
rs3804329
ATG5
1.000 0.080 6 106238552 intron variant A/G snv 0.15 2
rs3923594
MCAM
1.000 0.120 11 119317205 intron variant C/A;T snv 7.1E-06 2
rs4461062
NUP93
1.000 0.080 16 56830706 intron variant C/T snv 0.48 0.48 2
rs723526
EGFR
1.000 7 55067126 intron variant A/G snv 0.86 2
rs9397080
ESR1
1.000 0.040 6 152059380 intron variant C/T snv 0.22 2