Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs10894604
OPCML
11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs17213965
MYH11
16 15788110 intron variant C/T snv 0.24 1
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs6861681
CPEB4
5 173935455 intron variant G/A snv 0.22 1
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21 1
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs3088050
NSD1
5 177299634 3 prime UTR variant G/A snv 0.18 1
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs55747707
MLXIPL
7 73623036 intron variant G/A snv 0.16 1
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 3