Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 5
rs1057519901
FGFR2
0.925 0.080 10 121498525 missense variant T/G snv 5
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 5
rs786205228
PPP2R1A
0.827 0.080 19 52212718 missense variant C/G;T snv 3
rs1057519963
SOS1
0.925 0.080 2 39054637 missense variant T/A snv 2
rs1057519841
PIK3R1
0.925 0.120 5 68295269 missense variant A/G snv 5
rs387906678
FGFR2
0.851 0.120 10 121515263 missense variant A/C;G snv 5
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
rs1057519949
RHEB
0.851 0.120 7 151490964 missense variant A/T snv 4
rs1057519900
FGFR2
0.882 0.120 10 121515259 missense variant C/T snv 3
rs1057519968
SPOP ; LOC107984999
0.925 0.120 17 49619070 missense variant A/C;T snv 2
rs1057519969
LOC107984999 ; SPOP
0.925 0.120 17 49619069 missense variant C/G snv 2
rs1057519970
SPOP ; LOC107984999
0.925 0.120 17 49619068 missense variant C/A 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
rs1057519947
PPP2R1A
0.790 0.160 19 52212730 missense variant G/A snv 9
rs1057519893
ERBB3
0.790 0.160 12 56085070 missense variant G/A;T snv 8
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs1057519738
MIR4728 ; ERBB2
0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 7
rs1057519917
MTOR
0.807 0.160 1 11124517 missense variant A/G;T snv 7