Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 1
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 1
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs754688962
SF3B1
0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 3
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs1057520010
XPO1
0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
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
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 6
rs559063155
SF3B1
0.732 0.280 2 197402110 stop gained T/A;C;G snv 9.0E-05 1
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 8
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 10
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 15