Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 5
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs139236063
EGFR
0.925 0.080 7 55165350 missense variant G/C;T snv 3
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs387906589
ACVR1
0.925 0.120 2 157766004 missense variant C/A;T snv 3
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs779707422
FGFR1
0.763 0.280 8 38417331 missense variant G/A;T snv 4.0E-06 7
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs863224846
ACVR1
0.882 0.160 2 157770386 missense variant T/C;G snv 4.0E-06 3
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 9
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18