Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777900
MTOR
1.000 0.120 1 11114363 missense variant C/T snv 1
rs1057519780
MTOR
1.000 0.120 1 11127800 missense variant C/T snv 1
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 9
rs1057519958
RXRA
0.851 0.200 9 134436505 missense variant C/A;T snv 4
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 13
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 7
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs1057519950
RHEB
0.827 0.200 7 151490963 missense variant T/A;C snv 5
rs1057519949
RHEB
0.851 0.120 7 151490964 missense variant A/T snv 6
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
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 15
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12