Disease: Physical Activity Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1998710
LINC01720
1 190701754 intron variant C/T snv 0.57 2
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5
rs986732
CDH12
5 21918168 intron variant T/C snv 0.72 2
rs1934100 9 23234310 intron variant A/T snv 0.45 2
rs2044148
NCOA1
2 24514964 intron variant G/A snv 0.15 2
rs6752378 1.000 0.080 2 24927247 intergenic variant C/A snv 0.57 3
rs10510554
RARB
3 25058285 intron variant T/C snv 0.53 2
rs6804842
RARB
3 25064946 intron variant A/G snv 0.53 3
rs7619139
RARB
3 25068924 intron variant T/A snv 0.54 3
rs4858697
RARB
3 25075091 intron variant A/G snv 0.53 2
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs4923460
BDNF-AS ; LINC00678
11 27635242 intron variant G/T snv 0.20 3
rs2049045
BDNF-AS ; BDNF
1.000 0.080 11 27672694 intron variant G/A;C snv 0.13 3
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs10968577
LINGO2
9 28415514 intron variant C/T snv 0.27 3
rs2008514 16 28814284 non coding transcript exon variant G/A snv 0.35 3
rs12325113
ATXN2L
16 28837347 upstream gene variant T/C snv 0.28 2
rs4788102
SH2B1
0.851 0.160 16 28862077 intron variant G/A snv 0.34 6
rs1569980
LOC102724934
14 29215315 intron variant T/C snv 0.75 2
rs974471
LOC102724934
14 29216122 intron variant G/A snv 0.74 3
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4
rs17522122
AKAP6
0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41 5