Disease: Waist Circumference
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 9
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs6545714 2 59080590 intron variant G/A;C snv 4
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 3
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 3
rs16996700
LINC01524 ; LOC105372666
20 52365406 intron variant T/C snv 0.29 3
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21 3
rs929641
LINC01122
2 58565242 intron variant A/G snv 0.45 3
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 3