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
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
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
rs3822072
FAM13A
4 88820118 intron variant G/A;C 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
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
rs113313252
TNNI3K ; FPGT-TNNI3K ; LRRC53
1 74534327 intron variant -/T delins 2
rs12597579 16 20246545 intergenic variant C/A;T snv 2
rs12617233
LINC01122
2 58812863 intron variant T/A;C snv 2
rs12964056 18 60006567 upstream gene variant A/G;T snv 2
rs13386517 2 650479 regulatory region variant G/A;C snv 2
rs13386627 2 650560 regulatory region variant G/C;T snv 2
rs13388043 2 637597 regulatory region variant C/A;T snv 2
rs13393304 2 637830 regulatory region variant A/C;G snv 2
rs17124318
LINC01739
1 63015059 intron variant C/A;G;T snv 2
rs201167096
FPGT-TNNI3K ; LRRC53 ; TNNI3K
1 74534327 intron variant -/T delins 2
rs2272903
TFAP2B
6 50818858 5 prime UTR variant G/A;C snv 0.15 2