Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519887
EGFR
0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs769696078
EGFR
0.925 0.040 7 55154128 missense variant G/A snv 3
rs1057519830
EGFR
1.000 0.040 7 55163737 missense variant C/T snv 1
rs121909237
PTEN
1.000 0.040 10 87933121 missense variant C/G snv 1
rs121909250
ING1
1.000 0.040 13 110719736 missense variant G/C snv 1
rs121909251
ING1
1.000 0.040 13 110719739 missense variant A/G snv 1
rs121909252
ING1
1.000 0.040 13 110719667 missense variant C/A snv 1
rs121913433
EGFR
1.000 0.040 7 55174771 missense variant A/G snv 1
rs1057519951
RHOA
0.882 0.080 3 49375472 missense variant C/G;T snv 4
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 3
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 2
rs1057519905
H3C11
0.925 0.080 6 27872234 missense variant T/C snv 2
rs1131691036
TP53
0.851 0.080 17 7675207 frameshift variant GCA/CC delins 1
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 6
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 4
rs1057519948
RAC1
0.851 0.120 7 6387262 missense variant C/T snv 4
rs397514495
TP53
0.882 0.120 17 7675070 missense variant C/A;T snv 1.2E-05 4
rs1064793881
TP53
0.925 0.120 17 7673784 missense variant C/T snv 3
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 2
rs1567549584
TP53
0.925 0.120 17 7674245 missense variant T/C snv 2
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519938
PIK3CA
0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939
PIK3CA
0.776 0.160 3 179203763 missense variant A/C snv 10
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 10