Disease: Physical Activity Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
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
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 7
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 7
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 6
rs4715210 6 50929538 regulatory region variant C/G;T snv 4
rs7973683
CCDC92
12 123964676 intron variant C/A snv 0.39 3