Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6003
F13B
0.851 0.240 1 197061891 missense variant C/T snv 0.88 0.76 5
rs1498373
DDAH1
0.882 0.120 1 85324950 intron variant G/A snv 0.28 4
rs3737983
LRP8
0.851 0.120 1 53250744 missense variant G/A;T snv 0.40; 2.4E-05; 1.2E-05 4
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs6131
SELP
0.851 0.200 1 169611647 missense variant C/T snv 0.20 0.22 4
rs6133
SELP
0.851 0.280 1 169596108 missense variant C/A;G snv 0.12 4
rs10733113 0.882 0.160 1 247459055 upstream gene variant A/G snv 0.81 3
rs11572325
CYP2J2
0.925 0.080 1 59896030 intron variant A/T snv 0.12 3
rs1324214
F3
0.925 0.120 1 94531732 intron variant G/A snv 0.21 3
rs1361600
MIR12133 ; F3
0.925 0.120 1 94542362 upstream gene variant C/T snv 0.51 3
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs2298212
TNFRSF4
0.925 0.200 1 1211917 intron variant G/A snv 8.3E-02 8.0E-02 2
rs3917639 0.925 0.120 1 94527220 downstream gene variant C/T snv 2
rs867479748
SELP
0.925 0.160 1 169603047 missense variant C/T snv 2
rs9970807
PLPP3
0.925 0.080 1 56499992 intron variant C/T snv 0.11 2
rs10788952
LRP8
1.000 0.080 1 53272428 non coding transcript exon variant C/T snv 0.37 1
rs10889160
CYP2J2
1.000 0.080 1 59896449 intron variant T/C snv 0.23 1
rs1151640
OR13G1
1.000 0.080 1 247672648 missense variant T/C snv 0.46 0.36 1
rs12027041
LOC105378609 ; TP73
1.000 0.080 1 3674884 intron variant G/C snv 0.38 1
rs12118721
IL6R
1.000 0.080 1 154424940 intron variant T/C snv 0.51 1
rs13306731
SOAT1
1.000 0.080 1 179351443 missense variant A/G snv 0.11 6.9E-02 1
rs201977733
UTS2
1.000 0.080 1 7850908 missense variant C/T snv 5.6E-05 2.1E-05 1
rs2076059
SELE ; C1orf112
1.000 0.080 1 169729780 intron variant C/T snv 0.36 1
rs2271800
CYP2J2
1.000 0.080 1 59907994 intron variant A/C;T snv 1
rs2477786
DNAJC6
1.000 0.080 1 65266559 intron variant C/T snv 0.20 1