Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76165228
PPP1R14C
1.000 0.080 6 150198039 intron variant A/G;T snv 1
rs1564568660
PTEN
1.000 0.080 10 87961101 frameshift variant T/- delins 1
rs1923357
PTPRD
1.000 0.080 9 10266786 intron variant C/T snv 0.72 1
rs882380
SKAP1
1.000 0.080 17 48216874 intron variant C/A snv 0.52 1
rs1740828 0.925 0.080 6 21648854 regulatory region variant G/A snv 0.55 2
rs605965 0.925 0.080 6 75723198 downstream gene variant T/A snv 2.3E-02 2
rs2494737
AKT1
0.925 0.080 14 104779988 intron variant T/A snv 0.40 2
rs2494750
AKT1
0.925 0.080 14 104796575 upstream gene variant G/C snv 0.86 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
rs892119
AKT2 ; LOC107985289
0.925 0.080 19 40254165 intron variant C/T snv 0.19 2
rs4987886
ATM
0.925 0.080 11 108225326 5 prime UTR variant A/T snv 3.0E-02 2
rs3768235
BCL10
0.925 0.080 1 85267691 missense variant C/T snv 8.0E-06; 6.5E-02 4.5E-02 2
rs7579014
BCL11A
1.000 0.080 2 60480759 intron variant G/A snv 0.55 2
rs11196445
CASP7
0.925 0.080 10 113710131 intron variant G/A snv 0.11 2
rs10431923
CDH1
0.925 0.120 16 68805360 intron variant G/T snv 0.44 2
rs4783689
CDH1
0.925 0.080 16 68819768 intron variant C/T snv 0.30 2
rs3759216
CDKN1B ; GPR19
0.925 0.080 12 12715152 intron variant G/A snv 0.38 2
rs752760
CYP19A1
0.925 0.080 15 51339282 upstream gene variant C/T snv 0.57 2
rs2414098
CYP19A1 ; MIR4713HG
1.000 0.080 15 51245609 intron variant T/C snv 0.65 2
rs771432878
CYP1A1
0.925 0.080 15 74723013 missense variant A/G snv 4.0E-06 3.5E-05 2
rs140296720
DDR1
0.925 0.080 6 30896816 missense variant G/A snv 4.3E-06 2
rs757511141
DDX54 ; RITA1
0.925 0.080 12 113186886 missense variant C/G snv 8.0E-06 2.1E-05 2
rs10502289
ENOSF1
0.925 0.080 18 676789 intron variant A/T snv 0.15 2
rs2298581
ENOSF1
0.925 0.080 18 677931 intron variant C/G snv 0.22 2