Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 3
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs3088050
NSD1
5 177299634 3 prime UTR variant G/A snv 0.18 1
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 1
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 1
rs2076529
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs10894604
OPCML
11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs6931262
RREB1
6 7217284 non coding transcript exon variant C/T snv 0.10 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8