Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 16
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 15
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
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 12
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 11
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 10
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 8
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 8
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7