Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 1
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 5
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 1
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs290481
TCF7L2
0.827 0.200 10 113164066 intron variant C/T snv 0.20 1
rs11552449
AP4B1 ; DCLRE1B
0.925 0.080 1 113905767 missense variant C/G;T snv 0.22 0.15 2
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 1
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 1
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 13
rs1213469537
CAV1
0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 1
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv 1
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 11
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs1577074 10 118223544 intergenic variant A/G snv 0.16 1
rs10490913
LINC00867
10 118394924 intron variant T/C snv 0.39 1