Source: ALL
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: rs121913529
rs121913529
KRAS
144 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2015 2017
dbSNP: rs112445441
rs112445441
KRAS
32 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs121913237
rs121913237
NRAS
50 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs762846821
rs762846821
TP53
57 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs767741751
rs767741751
ANGPT2 ; MCPH1
5 0.851 0.120 8 6562846 missense variant C/A snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs770327175
rs770327175
CXCR4
5 0.851 0.120 2 136115878 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs914956206
rs914956206
VEGFA
4 0.882 0.080 6 43770762 missense variant G/A;T snv 0.010 1.000 1 2015 2015