Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 3
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 1
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs6942652
CPED1
7 121249218 intron variant G/C;T snv 1
rs6931262
RREB1
6 7217284 non coding transcript exon variant C/T snv 0.10 1
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs6861681
CPEB4
5 173935455 intron variant G/A snv 0.22 1
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs6784615
NISCH
1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1
rs6701231
TBX15
1 118953038 intron variant C/A;G snv 1
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs6486060
NRIP3 ; LOC105376541
11 9003083 intron variant G/A snv 0.55 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs634869 6 139510620 intron variant T/A;C snv 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs620861
PCAT1 ; CASC8 ; POU5F1B ; CASC21
0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs605203
EHMT2-AS1 ; LOC107986588 ; CYP21A2 ; SLC44A4
1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs55747707
MLXIPL
7 73623036 intron variant G/A snv 0.16 1
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 1
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 1