Disease: Physical Activity Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs10510554
RARB
3 25058285 intron variant T/C snv 0.53 2
rs10923724 1 119004219 upstream gene variant C/T snv 0.53 3
rs10968577
LINGO2
9 28415514 intron variant C/T snv 0.27 3
rs11209951
LOC105378797
1 72371807 intron variant C/T snv 0.61 3
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
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
rs12325113
ATXN2L
16 28837347 upstream gene variant T/C snv 0.28 2
rs12406019 1 78212446 intergenic variant A/G snv 0.32 2
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs12641981 4 45177866 intergenic variant C/T snv 0.37 2
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4
rs1308362
MRAS
3 138385085 intron variant A/G;T snv 2
rs13191362
PRKN
6 162612318 intron variant A/G snv 8.7E-02 3
rs1381660 8 75961464 intergenic variant A/G snv 0.63 2
rs1569980
LOC102724934
14 29215315 intron variant T/C snv 0.75 2
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs1707322 1 46039475 downstream gene variant A/G snv 0.68 2
rs1720825
MRAS
3 138389241 intron variant A/G;T snv 2
rs17405819 8 75894349 intergenic variant T/C snv 0.24 3
rs1808192 17 47717340 regulatory region variant A/G snv 0.69 2
rs185350
KCTD15
19 33815911 downstream gene variant C/T snv 0.44 2
rs1884897 20 6632185 regulatory region variant A/G;T snv 5