Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1277240795
OGA
1.000 0.040 10 101791382 missense variant G/C snv 7.0E-06 2
rs1709393
LINC02085
1.000 0.080 3 101980310 intron variant C/T snv 0.55 2
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs4623951
DAO
0.925 0.080 12 108878275 intron variant C/G;T snv 3
rs2070587
DAO
0.882 0.080 12 108883967 intron variant T/G snv 0.32 5
rs2111902
DAO
0.925 0.080 12 108884971 intron variant T/A;G snv 0.40 3
rs3741775
DAO
0.925 0.080 12 108889827 intron variant A/C;G snv 3
rs11669576
LDLR ; MIR6886
0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 6
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2572431 1.000 0.040 8 11247568 downstream gene variant C/G;T snv 2
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1012176
CTNND2
5 11320426 intron variant G/T snv 0.24 1
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs1110976
DRD2
1.000 0.040 11 113413797 intron variant T/G snv 3
rs4245146
DRD2
1.000 0.040 11 113447251 intron variant T/C snv 0.49 3
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6330
NGF ; NGF-AS1
0.763 0.240 1 115286692 missense variant G/A snv 0.37 0.36 12
rs10112596
GATA4
0.925 0.120 8 11722293 intron variant A/G snv 0.83 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs8192506
DBI
1.000 0.040 2 119372265 missense variant A/C;G snv 4.0E-06; 2.5E-02 2
rs3817190
CAMKK2
0.851 0.080 12 121274274 missense variant T/A;G snv 0.38 6
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs56242606
VWDE
1.000 0.040 7 12382283 intron variant T/C snv 5.3E-02 2
rs10893268
OR8A1
11 124568716 intron variant C/T snv 0.40 1