Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs11231111
AHNAK
11 62492533 intron variant C/T snv 0.15 2
rs11231693
MACROD1 ; FLRT1
11 64095140 intron variant G/A snv 0.11 2
rs113313252
TNNI3K ; FPGT-TNNI3K ; LRRC53
1 74534327 intron variant -/T delins 2
rs11671664
GIPR
0.925 0.120 19 45669020 intron variant G/A snv 0.12 2
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 2
rs1167800
HIP1
7 75546898 intron variant A/G snv 0.34 2
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 2
rs11951673
LOC101929710 ; CAST
5 96525308 non coding transcript exon variant C/T snv 0.39 2
rs1211166
NTRK2
9 84671077 intron variant G/A snv 0.77 2
rs12142020
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1 74534327 intron variant A/T snv 0.50 2
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 4
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs12444979
LOC105371116
1.000 0.080 16 19922278 intergenic variant C/T snv 0.11 2
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 3
rs12525532
ANKS1A
6 35037042 intron variant C/T snv 0.33 2
rs12597579 16 20246545 intergenic variant C/A;T snv 2
rs12617233
LINC01122
2 58812863 intron variant T/A;C snv 2
rs12714414 2 651407 intergenic variant T/C snv 0.18 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 1
rs12964056 18 60006567 upstream gene variant A/G;T snv 2
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs12999687
DNMT3A
2 25289569 intron variant T/G snv 0.48 2
rs13013484 2 27765954 intergenic variant G/A snv 0.61 3