Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21 1
rs6861681
CPEB4
5 173935455 intron variant G/A snv 0.22 1
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs17213965
MYH11
16 15788110 intron variant C/T snv 0.24 1
rs10894604
OPCML
11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 1
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs4640244
KCNJ12
17 21380911 intron variant A/G snv 0.33 1
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 1
rs1254319
C14orf39
1.000 14 60437039 missense variant G/A snv 0.35 0.36 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs620861
PCAT1 ; CASC8 ; POU5F1B ; CASC21
0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs7637773
IGF2BP2
1.000 0.080 3 185797847 intron variant G/A snv 0.38 1