Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
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
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
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 3
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3