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
rs10923724 1 119004219 upstream gene variant C/T snv 0.53 3
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
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
rs12969709 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 4
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs1381660 8 75961464 intergenic variant A/G snv 0.63 2
rs1707322 1 46039475 downstream gene variant A/G snv 0.68 2
rs17405819 8 75894349 intergenic variant T/C snv 0.24 3
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1808192 17 47717340 regulatory region variant A/G snv 0.69 2
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs1928295 9 117616205 intergenic variant T/C snv 0.45 3
rs1934100 9 23234310 intron variant A/T snv 0.45 2
rs2008514 16 28814284 non coding transcript exon variant G/A snv 0.35 3
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs2546057 1.000 0.040 19 33829949 intergenic variant A/C snv 0.41 3
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs29943 19 33817305 downstream gene variant T/C snv 0.70 2
rs3843262 1 74547370 downstream gene variant T/A snv 0.52 2
rs4146429 10 102641875 upstream gene variant T/C snv 0.10 2
rs4715210 6 50929538 regulatory region variant C/G;T snv 4