Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 9
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1060501687
ATM
0.925 0.320 11 108272782 stop gained G/T snv 4.0E-06 7.0E-06 2
rs1060502333
BRCA1
0.882 0.200 17 43093322 frameshift variant T/- delins 3
rs1060502787
PALB2
0.925 0.160 16 23626399 splice acceptor variant T/C;G snv 2
rs1064793732
PIK3CA
0.882 0.320 3 179204536 missense variant G/A snv 3
rs1064793881
TP53
0.925 0.120 17 7673784 missense variant C/T snv 3
rs1064793887
BRIP1
0.925 0.240 17 61743135 splice acceptor variant C/T snv 2
rs1064793929
TP53
0.882 0.280 17 7675167 frameshift variant A/-;AA delins 5
rs1064796722
TP53
1.000 0.120 17 7676043 missense variant A/C;G snv 1
rs10674174 1.000 0.120 13 61317942 intergenic variant -/G ins 1
rs10858374
LOC107987138
1.000 0.120 9 135247660 intron variant T/C snv 0.37 1
rs10899426 1.000 0.120 11 78008566 intergenic variant T/C snv 3.3E-02 1
rs10962692 0.925 0.120 9 16915876 upstream gene variant G/A;C snv 3
rs11084033
LOC105372441
0.882 0.120 19 50850699 intron variant C/A;T snv 4
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs1114167776
MSH6 ; FBXO11
1.000 0.120 2 47791020 frameshift variant -/T delins 2
rs111478044
NCAM2
1.000 0.120 21 21308069 intron variant TA/-;TATA delins 1
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17