Disease: Physical Activity Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs4788102
SH2B1
0.851 0.160 16 28862077 intron variant G/A snv 0.34 6
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 6
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs17522122
AKAP6
0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4
rs12969709 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4