Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36217263
KL
1.000 0.040 13 33015697 upstream gene variant A/- del 0.21 4
rs9319428
FLT1
0.925 0.080 13 28399484 intron variant G/A snv 0.30 4
rs1289389
SLC15A1
13 98684036 3 prime UTR variant C/T snv 0.18 2
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs4363657
SLCO1B1
12 21215788 intron variant T/C snv 0.18 5
rs739837
VDR
0.882 0.200 12 47844438 3 prime UTR variant G/C;T snv 5
rs11066782
KCTD10
1.000 0.040 12 109472747 intron variant C/T snv 0.17 2
rs11067233
MMAB
1.000 0.040 12 109556403 3 prime UTR variant C/G snv 0.23 0.24 2
rs11613718
KCTD10
1.000 0.040 12 109474527 intron variant C/T snv 0.17 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs670
APOA1 ; APOA1-AS
0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8
rs11039155
NR1H3
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12 6
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 5
rs633389 1.000 0.040 11 116796621 upstream gene variant C/T snv 0.13 4
rs10892151
DSCAML1 ; LOC105369515
1.000 11 117661016 intron variant C/T snv 9.7E-02 3