Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs10894604
OPCML
11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 1
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 3
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs1876829
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs2076529
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs1294410
LOC101928004
6 6738519 intron variant T/C snv 0.65 1
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs634869 6 139510620 intron variant T/A;C snv 2
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 1
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1