Disease: Physical Activity Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1308362
MRAS
3 138385085 intron variant A/G;T snv 2
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs1720825
MRAS
3 138389241 intron variant A/G;T snv 2
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs2035935
RASA2
3 141587171 intron variant A/G;T snv 2
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs40067
FBXL17
5 108103311 intron variant G/A;T snv 2
rs4715210 6 50929538 regulatory region variant C/G;T snv 4
rs6864049
LOC105379158 ; LINC02240
5 124994829 intron variant A/C;G;T snv 2
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs7164727 15 72801650 downstream gene variant C/G;T snv 3
rs754635
CCK
1.000 0.040 3 42263639 splice region variant C/G;T snv 0.84; 5.6E-06 3
rs7550173
LOC105378797
1 72478934 intron variant A/C;T snv 2
rs757318
CRTC1
19 18709498 intron variant C/A;G;T snv 3
rs7715806 5 75738562 intergenic variant C/G;T snv 3
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9469913
UHRF1BP1
6 34859308 missense variant A/G;T snv 4.0E-06; 0.16 2
rs984222
TBX15
1 118961220 intron variant C/A;G snv 3
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs7550711
GPR61
1 109540264 intron variant C/T snv 2.6E-02 3
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs13191362
PRKN
6 162612318 intron variant A/G snv 8.7E-02 3
rs4146429 10 102641875 upstream gene variant T/C snv 0.10 2