Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
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
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 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
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 3