Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 1
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 1
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs1254319
C14orf39
1.000 14 60437039 missense variant G/A snv 0.35 0.36 1
rs1406948
UQCC1
20 35317816 intron variant G/A snv 0.44 1
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 1
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21 1
rs3088050
NSD1
5 177299634 3 prime UTR variant G/A snv 0.18 1
rs55747707
MLXIPL
7 73623036 intron variant G/A snv 0.16 1
rs620861
PCAT1 ; CASC8 ; POU5F1B ; CASC21
0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs6486060
NRIP3 ; LOC105376541
11 9003083 intron variant G/A snv 0.55 1
rs6861681
CPEB4
5 173935455 intron variant G/A snv 0.22 1
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 1