Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
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
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 3
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 3
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 3
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 3
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 2
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 2
rs12597579 16 20246545 intergenic variant C/A;T snv 2
rs12964056 18 60006567 upstream gene variant A/G;T snv 2
rs17124318
LINC01739
1 63015059 intron variant C/A;G;T snv 2
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2