Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs3803304
AKT1
0.882 0.160 14 104772809 intron variant C/G snv 0.24 3
rs2494740
AKT1
0.925 0.080 14 104781544 intron variant A/T snv 0.61 2
rs2494744
AKT1
0.925 0.080 14 104789477 intron variant A/G snv 0.83 2
rs2498789
AKT1
0.925 0.080 14 104783708 intron variant A/G snv 0.26 2