Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 5
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 5
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 4
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 4
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 4
rs4691380
PDGFC
4 156798972 intron variant C/T snv 0.45 4
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 4
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 4
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 3
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 3
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 3
rs13273088
SULF1
8 69581739 intron variant G/A snv 0.81 3
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 3