Source: ALL
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
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs17507636
CTB-30L5.1
1.000 0.160 7 106650672 intron variant C/T snv 0.23 1
rs1555902 1.000 0.160 13 108204435 downstream gene variant C/A snv 0.10 1
rs104894419
LIG4
0.807 0.360 13 108208829 stop gained G/A snv 9.9E-05 7.0E-05 8
rs193451 1.000 0.160 7 108670542 intergenic variant A/G snv 0.36 1
rs12711846
MIR4435-2HG ; ACOXL-AS1 ; ACOXL
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26 4
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs121918465
PTPN11
0.827 0.200 12 112450407 missense variant A/C;G;T snv 7
rs397507546
PTPN11
0.790 0.360 12 112489084 missense variant G/A;C;T snv 9
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
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
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 17
rs6595443
CEP120
1.000 0.160 5 123407631 intron variant A/T snv 0.44 1
rs4525246
GRAMD1B
0.851 0.160 11 123524538 intron variant G/A;C snv 4
rs58618031
POT1-AS1
1.000 0.160 7 124943842 intron variant T/C snv 0.24 1