Disease: Physical Activity Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
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
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 7
rs849140
JAZF1
0.851 0.240 7 28144083 intron variant T/C snv 0.58 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 6
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 6
rs10804591 3 129615390 intergenic variant C/A snv 0.63 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5