Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs833070
VEGFA
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 3
rs35542019
LINC00649 ; LOC101928126
21 33974555 non coding transcript exon variant AA/-;A delins 0.57 3
rs632057 6 139512875 intron variant T/G snv 0.57 3
rs442177
AFF1
4 87109109 intron variant G/T snv 0.56 4
rs2303566
STK36
2 218693015 intron variant G/A;T snv 0.56 2
rs1936807
RSPO3
6 127127104 intron variant C/G snv 0.55 4
rs11122272
EXOC8
1 231335026 3 prime UTR variant A/G snv 0.55 1
rs5758896
A4GALT
22 42719570 intron variant T/C snv 0.55 3
rs2230657
NASP
1 45607817 synonymous variant G/A snv 0.52 0.55 1
rs66782572
NT5DC2
3 52533601 missense variant A/G snv 0.48 0.51 1
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs554019
DNM3
1 172171408 intron variant C/T snv 0.49 1
rs1340818
POMP
13 28665493 intron variant T/C snv 0.48 1
rs806293
DLEU1
13 50238846 intron variant T/A snv 0.47 2
rs4580814
SLC12A7 ; LOC105374612
5 1113129 upstream gene variant G/T snv 0.47 2
rs57908212
AP3D1
19 2161322 intron variant T/C snv 0.46 3
rs12982593
DOT1L
19 2175892 intron variant C/A snv 0.46 1
rs11072566
NRG4
0.925 0.120 15 76001630 intron variant A/G snv 0.45 2
rs10494964
LOC105372912
1 213793544 intron variant T/C snv 0.45 2
rs3996993
GSTA11P
6 52860723 intron variant T/C snv 0.44 1
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs56235845
RGS14
5 177371039 splice region variant T/G snv 0.36 0.42 2
rs9260313
HLA-A
6 29949108 downstream gene variant T/C snv 0.42 2
rs4791641
PFAS
17 8257831 missense variant C/T snv 0.43 0.41 4
rs34477782
LOC105374292 ; LINC01968
3 194785474 intron variant CT/- del 0.41 2