Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 17
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 12
rs1057519886
CTNNB1
0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv 6
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 13
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 11
rs1057519890
ERBB2
0.807 0.200 17 39723966 missense variant T/A snv 8
rs121913468
ERBB2
0.827 0.160 17 39724008 missense variant G/A;C;T snv 7
rs1057519862
ERBB2
0.851 0.160 17 39723405 missense variant G/A snv 5
rs1057519893
ERBB3
0.790 0.160 12 56085070 missense variant G/A;T snv 9
rs1057519891
ERBB3
0.851 0.160 12 56088557 missense variant G/A;T snv 4.0E-06 6
rs1057519892
ERBB3
0.851 0.160 12 56088558 missense variant A/T snv 5
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 15
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs747241612
FBXW7
0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs1057519897
FGFR1
0.807 0.240 8 38414788 missense variant C/G;T snv 4.0E-06 6
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 45
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 18