Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs1250566
ZMIZ1
10 79286696 intron variant G/A snv 0.24 1
rs1250569
ZMIZ1
0.925 0.040 10 79285450 intron variant T/C snv 0.44 0.51 3
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 3
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs2160322
MAGI2
0.851 0.160 7 78462650 intron variant G/A;C snv 5
rs6962966
MAGI2
0.925 0.120 7 78174806 intron variant A/G snv 0.50 3
rs1248696
DLG5
0.807 0.080 10 77856847 missense variant T/A;C snv 0.93 8
rs1333407770
DLG5
0.925 0.040 10 77811115 frameshift variant G/-;GG delins 3
rs2289310
DLG5
0.925 0.040 10 77811115 missense variant G/A;C;T snv 4.0E-06; 8.0E-06; 5.7E-02 3
rs2165047
DLG5
1.000 0.040 10 77791882 3 prime UTR variant C/T snv 0.26 2
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs34694289
FCER2
19 7689215 missense variant G/A;C snv 2.4E-03; 1.6E-05 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs6817952
ART3 ; CXCL11
4 76035890 intron variant G/A;T snv 0.16; 4.3E-06 1
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs17000400 4 75251521 regulatory region variant C/T snv 0.12 1
rs4899554 14 75234518 downstream gene variant C/T snv 0.14 1
rs2395128
DUPD1
1.000 0.040 10 75052692 intron variant G/T snv 0.32 2
rs2472649 4 73991991 upstream gene variant A/G;T snv 1
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs2688608 1.000 0.080 10 73898591 regulatory region variant G/T snv 0.44 2
rs10061469 5 73222321 intron variant T/C snv 0.37 1