Disease: Physical Activity Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1928295 9 117616205 intergenic variant T/C snv 0.45 3
rs1934100 9 23234310 intron variant A/T snv 0.45 2
rs1998710
LINC01720
1 190701754 intron variant C/T snv 0.57 2
rs2008514 16 28814284 non coding transcript exon variant G/A snv 0.35 3
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs2035935
RASA2
3 141587171 intron variant A/G;T snv 2
rs2044148
NCOA1
2 24514964 intron variant G/A snv 0.15 2
rs2075171
LINC01122
2 58461772 splice region variant G/A snv 0.18 2
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs2245368
DTX2P1-UPK3BP1-PMS2P11 ; LOC105375361
7 76978826 non coding transcript exon variant C/T snv 0.80 3
rs2303108
ZC3H4
19 47086638 intron variant T/C snv 0.63 3
rs2365389
FHIT
3 61250788 intron variant C/T snv 0.56 3
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2395607
UHRF1BP1
6 34805950 intron variant C/T snv 0.22 2
rs2430307
DTX2P1-UPK3BP1-PMS2P11
7 76980627 non coding transcript exon variant T/C snv 0.79 2
rs2590838
PBRM1
3 52588070 intron variant G/A snv 0.55 3
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs29943 19 33817305 downstream gene variant T/C snv 0.70 2
rs3732869
RASA2
3 141576936 intron variant T/A snv 0.13 2
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs3843262 1 74547370 downstream gene variant T/A snv 0.52 2
rs40067
FBXL17
5 108103311 intron variant G/A;T snv 2
rs4146429 10 102641875 upstream gene variant T/C snv 0.10 2
rs4234589
ETV5
3 186101093 intron variant A/G snv 0.13 2
rs4498364
MMS22L
6 97165897 intron variant C/T snv 0.74 2