Disease: Physical Activity Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs2546057 1.000 0.040 19 33829949 intergenic variant A/C snv 0.41 3
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs6864049
LOC105379158 ; LINC02240
5 124994829 intron variant A/C;G;T snv 2
rs7550173
LOC105378797
1 72478934 intron variant A/C;T snv 2
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs12406019 1 78212446 intergenic variant A/G snv 0.32 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
rs1707322 1 46039475 downstream gene variant A/G snv 0.68 2
rs1808192 17 47717340 regulatory region variant A/G snv 0.69 2
rs4234589
ETV5
3 186101093 intron variant A/G snv 0.13 2
rs4858697
RARB
3 25075091 intron variant A/G snv 0.53 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs6804842
RARB
3 25064946 intron variant A/G snv 0.53 3
rs7175517
MAP2K5
15 67785292 intron variant A/G snv 0.30 2
rs7526762
LRRC53 ; TNNI3K ; FPGT-TNNI3K
1 74527634 intron variant A/G snv 0.42 2
rs759250 2 59102018 intron variant A/G snv 0.80 2
rs7864204
TMEM252-DT
9 68614263 intron variant A/G snv 0.61 2
rs935111 3 42273163 intergenic variant A/G snv 0.88 2
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs1308362
MRAS
3 138385085 intron variant A/G;T snv 2
rs1720825
MRAS
3 138389241 intron variant A/G;T snv 2
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2035935
RASA2
3 141587171 intron variant A/G;T snv 2