Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 42
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 29
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 14
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 7
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 6
rs121913248
NRAS
1.000 0.040 1 114716109 missense variant C/G;T snv 4.0E-06 1