Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201227909
AKT1
0.925 0.160 14 104770839 synonymous variant T/C snv 2
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs1042852
CBLB
1.000 0.080 3 105658671 3 prime UTR variant C/G;T snv 1
rs2305035
CBLB
1.000 0.080 3 105720182 synonymous variant G/A snv 0.22 0.21 2
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 3
rs2245214
ATG5
0.827 0.240 6 106214866 intron variant C/G snv 0.42 6
rs776310470
DAP
1.000 0.080 5 10680713 synonymous variant G/A snv 4.6E-04 5.8E-04 1
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs1805329
RAD23B
0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 15
rs372514872
RAD23B
1.000 0.080 9 107322086 missense variant C/T snv 2.0E-05 3.5E-05 1
rs1805388
LIG4
0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs228590
ATM
1.000 0.080 11 108225414 5 prime UTR variant A/G snv 0.52 1
rs1878022
CMKLR1
0.851 0.080 12 108305255 intron variant C/T snv 0.70 4
rs227060
C11orf65 ; ATM
0.882 0.160 11 108334154 intron variant C/T snv 0.27 3
rs170548
ATM ; C11orf65
1.000 0.080 11 108364109 intron variant A/C;T snv 1
rs4978754
ELP1
0.851 0.080 9 108884801 intron variant T/C snv 0.92 4
rs11080466
PIEZO2
1.000 0.080 18 10899030 intron variant A/G snv 0.31 1
rs748625642
MMAB
0.925 0.200 12 109568774 missense variant T/C snv 4.0E-06 2
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs6822976
CFI
1.000 0.080 4 109745136 intron variant G/A snv 0.41 1
rs7671905
CFI
1.000 0.080 4 109801730 intron variant T/C snv 0.64 1
rs778040733
EGF
1.000 0.080 4 109988662 missense variant T/C snv 1.2E-05 1.4E-05 1