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
rs1130233
AKT1
0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs2498801
LOC102723342 ; AKT1
0.790 0.120 14 104769221 upstream gene variant T/C snv 0.41 7
rs1200003171
AKT1
0.882 0.120 14 104775122 missense variant C/A;T snv 8.0E-06 4
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
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
rs1038322721
AKT1
1.000 0.080 14 104775774 missense variant T/C snv 7.0E-06 1