Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 3
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 2
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
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
rs634869 6 139510620 intron variant T/A;C snv 2
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 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
rs1034207 6 127016554 intron variant C/A;G;T snv 0.94 1
rs10894604
OPCML
11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs11154370 6 126846446 intron variant A/G;T snv 1
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 1