Source: BEFREE ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121913238
rs121913238
KRAS
14 0.732 0.240 12 25227343 missense variant G/C;T snv 0.010 1.000 1 2016 2016
dbSNP: rs121913250
rs121913250
NRAS
14 0.683 0.440 1 114716127 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs121913254
rs121913254
NRAS
29 0.658 0.440 1 114713909 stop gained G/A;C;T snv 0.010 1.000 1 2016 2016
dbSNP: rs121913530
rs121913530
KRAS
55 0.583 0.640 12 25245351 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs63751428
rs63751428
MLH1
1 0.882 0.160 3 36996686 stop gained C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs876660952
rs876660952
MLH1
1 1.000 0.040 3 37028854 missense variant T/G snv 4.0E-06 0.010 1.000 1 2016 2016