Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 13
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs12967135 18 60181790 intergenic variant G/A snv 0.24 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs9813495
CADM2
3 85777231 intron variant A/G snv 0.15 4
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 4
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 4
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 3
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 3
rs42377
CDK6
7 92614358 3 prime UTR variant G/A snv 0.28 3
rs12146733
FAIM2
12 49876581 intron variant G/C;T snv 3
rs1916799
FHIT
3 61247301 intron variant G/A;T snv 3
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 3
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 3
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 3
rs10198628 2 12824371 intron variant A/G snv 0.59 2
rs11863065 16 82293200 intergenic variant G/A snv 7.3E-02 2