Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs2295080
MTOR
0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs7483
GSTM3 ; GSTM5
0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs3021097
IL10 ; IL19
0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs587777894
MTOR
0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs1057519917
MTOR
0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs1131691061
SDHB
0.827 0.280 1 17054017 start lost C/T snv 6
rs1332018
GSTM5 ; GSTM3
0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv 5
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv 5
rs1057519916
MTOR
0.882 0.160 1 11109320 missense variant T/A snv 4
rs786205165
MTOR
0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv 3
rs11203289
SDHB
0.882 0.240 1 17054012 missense variant G/A;C snv 4.1E-06; 3.1E-03 3
rs2050462
CSF1
0.925 0.120 1 109930334 3 prime UTR variant T/A;G snv 2
rs333951
CSF1
0.925 0.120 1 109909068 upstream gene variant T/C snv 0.74 2
rs3889728
AGT
1.000 0.120 1 230713085 intron variant C/T snv 0.24 2
rs4381241
FAF1
0.925 0.120 1 50441766 intron variant T/C snv 0.51 2