Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143267032
CUX1
1.000 0.160 7 102028117 missense variant C/G snv 2.8E-05 2.8E-05 1
rs12147254
TRAF3
0.851 0.240 14 102799329 intron variant G/A snv 0.23 4
rs764931115
AKT1
0.925 0.200 14 104780148 missense variant T/C snv 4.0E-06 3
rs1555902 1.000 0.160 13 108204435 downstream gene variant C/A snv 0.10 1
rs193451 1.000 0.160 7 108670542 intergenic variant A/G snv 0.36 1
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 19
rs121918465
PTPN11
0.827 0.200 12 112450407 missense variant A/C;G;T snv 1
rs397507546
PTPN11
0.790 0.360 12 112489084 missense variant G/A;C;T snv 2
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 7
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 6
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 42
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 14
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
rs2228055
IL10RA
0.851 0.280 11 117994131 missense variant A/C;G snv 8.2E-02 4
rs121913478
FGFR2
0.708 0.640 10 121515280 missense variant T/C snv 5
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 16
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 3
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
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-06 484
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 7
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 14