Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs605203
EHMT2-AS1 ; LOC107986588 ; CYP21A2 ; SLC44A4
1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 2
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 2
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 1
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 1
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs2894204
HLA-C
1.000 0.040 6 31269284 intron variant C/A;T snv 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 1
rs7637773
IGF2BP2
1.000 0.080 3 185797847 intron variant G/A snv 0.38 1
rs4640244
KCNJ12
17 21380911 intron variant A/G snv 0.33 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs1876829
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs1294410
LOC101928004
6 6738519 intron variant T/C snv 0.65 1
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs987763
LOC105377989
6 126960402 intron variant C/A;T snv 1