Disease: Lean body mass
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 5
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs12284933
PPP6R3
11 68552021 intron variant G/A snv 0.23 2
rs12741884 1 22268202 downstream gene variant G/A;C snv 2
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 2
rs2955382
GID4
17 18044396 intron variant C/T snv 0.43 2
rs3765350
WNT4
1 22120823 intron variant A/G snv 0.22 2
rs6726821 2 165721604 intergenic variant T/G snv 0.40 2
rs7501812
TOM1L2
17 17847593 3 prime UTR variant G/A snv 0.47 0.52 2
rs7672749 4 87877132 intergenic variant G/A snv 0.11 2
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33 2
rs9525638 13 42554441 regulatory region variant T/C snv 0.37 2