Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs749415085
PIK3CA
0.807 0.160 3 179198937 missense variant C/A;G;T snv 7
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs747241612
FBXW7
0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs74535574
APC
5 112839879 stop gained C/A;T snv 1
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs727502902
BRAF
0.882 0.080 7 140753338 inframe insertion -/TAG delins 4.0E-06 4
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 14
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 11
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs587777894
MTOR
0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 1
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs398124146
CREBBP
0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11