Disease: Physical Activity Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs2049045
BDNF-AS ; BDNF
1.000 0.080 11 27672694 intron variant G/A;C snv 0.13 3
rs4234589
ETV5
3 186101093 intron variant A/G snv 0.13 2
rs3732869
RASA2
3 141576936 intron variant T/A snv 0.13 2
rs6809651
ETV5
3 186096853 intron variant G/A snv 0.14 4
rs9852859
CADM2
3 85793191 intron variant T/C snv 0.15 2
rs2044148
NCOA1
2 24514964 intron variant G/A snv 0.15 2
rs9852127
CADM2
3 85777586 intron variant G/A snv 0.15 2
rs943005 6 50898107 non coding transcript exon variant C/T snv 0.16 3
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 5
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs2075171
LINC01122
2 58461772 splice region variant G/A snv 0.18 2
rs587242 1 96420711 downstream gene variant G/A snv 0.19 2
rs9818122
CADM2 ; CADM2-AS2
3 85811914 intron variant T/C snv 0.20 2
rs4923460
BDNF-AS ; LINC00678
11 27635242 intron variant G/T snv 0.20 3
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs12969709 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 4
rs7757419
PACSIN1
6 34471792 intron variant A/T snv 0.22 2
rs2395607
UHRF1BP1
6 34805950 intron variant C/T snv 0.22 2
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5