Disease: Polysomnography
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs3741298
ZPR1
11 116786845 intron variant C/T snv 0.73 3