Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145929329
CDKN2B-AS1
0.882 0.040 9 22066213 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT delins 0.58 1
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 1
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 1
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 1
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 1
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 1
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 1
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 1
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 1
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 1
rs6062302
RTEL1 ; RTEL1-TNFRSF6B
0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81 1
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 1
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 1
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 1
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 1
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 1
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 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
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 1
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 1
rs2291427
ALOX5
0.925 0.040 10 45440776 intron variant A/G;T snv 2
rs11548193
BCAT2
0.925 0.040 19 48799813 missense variant G/A;C snv 0.14 2