Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1492078
AGTR1
1.000 0.120 3 148697390 upstream gene variant T/C snv 0.50 1
rs375129361
BAP1
0.925 0.120 3 52408056 missense variant T/A;C snv 4.1E-06 1
rs1800645
CALB1
1.000 0.120 8 90083245 intron variant A/G;T snv 1
rs1944129
CCND1
1.000 0.120 11 69639167 upstream gene variant C/G;T snv 1
rs121913668
MET
0.882 0.120 7 116778827 missense variant T/C snv 1
rs121913671
MET
0.882 0.160 7 116783353 missense variant G/A;C snv 1
rs121913673
MET
0.925 0.120 7 116782048 missense variant C/G;T snv 1
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 1
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 1
rs1057519950
RHEB
0.827 0.200 7 151490963 missense variant T/A;C snv 1
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 1
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 1
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 1
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 1
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 1
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 1
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 1
rs11813268 0.925 0.120 10 103922538 upstream gene variant C/T snv 0.31 2
rs1417080 0.925 0.120 9 79515946 non coding transcript exon variant T/C snv 0.35 2
rs3118523 0.925 0.120 9 134443675 downstream gene variant G/A snv 0.75 2
rs6466135 0.925 0.120 7 106861053 upstream gene variant A/G snv 0.71 2
rs7132434 0.925 0.120 12 26319629 non coding transcript exon variant A/G snv 0.62 2
rs748964 0.925 0.120 9 134442243 downstream gene variant C/G;T snv 2
rs1154454
ADH7
0.925 0.120 4 99417185 intron variant A/G snv 0.22 2
rs3889728
AGT
1.000 0.120 1 230713085 intron variant C/T snv 0.24 2