Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1038322721
AKT1
1.000 0.080 14 104775774 missense variant T/C snv 7.0E-06 1
rs11847866
AKT1
1.000 0.040 14 104788868 intron variant G/A snv 0.30 1
rs1361898625
AKT1
1.000 0.040 14 104776718 synonymous variant G/A snv 1
rs1380514442
AKT1
14 104780205 missense variant T/C snv 4.0E-06 1
rs2494738
AKT1
1.000 0.080 14 104780349 intron variant G/A snv 1.0E-01 1
rs2494746
AKT1
1.000 0.080 14 104791382 intron variant C/G snv 0.77 1
rs2498796
AKT1
1.000 0.080 14 104776883 non coding transcript exon variant G/A snv 0.33 1
rs397514645
AKT1
1.000 14 104770805 missense variant T/G snv 1
rs61759760
AKT1
14 104789850 intron variant C/T snv 0.31 1
rs1057519804
AKT1
1.000 0.040 14 104776711 missense variant G/T snv 2
rs201227909
AKT1
0.925 0.160 14 104770839 synonymous variant T/C snv 2
rs2494737
AKT1
0.925 0.080 14 104779988 intron variant T/A snv 0.40 2
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
rs2494748
AKT1
14 104792555 intron variant C/T snv 0.51 0.48 2
rs2494750
AKT1
0.925 0.080 14 104796575 upstream gene variant G/C snv 0.86 2
rs2498786
AKT1
0.925 0.160 14 104796031 upstream gene variant C/G snv 0.50 2
rs2498789
AKT1
0.925 0.080 14 104783708 intron variant A/G snv 0.26 2
rs2498794
AKT1
14 104778914 intron variant A/G snv 0.54 2
rs2498799
AKT1
0.925 0.040 14 104773557 synonymous variant C/T snv 2
rs397514644
AKT1
0.925 0.040 14 104780190 missense variant G/A snv 7.0E-06 2
rs72715985
AKT1
0.925 0.080 14 104797210 upstream gene variant C/T snv 2.6E-02 2
rs74090038
AKT1
0.925 0.080 14 104796444 upstream gene variant C/T snv 0.29 2
rs3803304
AKT1
0.882 0.160 14 104772809 intron variant C/G snv 0.24 3
rs764931115
AKT1
0.925 0.200 14 104780148 missense variant T/C snv 4.0E-06 3