Disease: Lean body mass
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2900208
ETV6
12 11725530 intron variant C/A snv 0.29 2
rs12509014
NUDT6
4 122904764 intron variant C/T snv 0.63 2
rs4870941 8 125486586 intron variant G/C snv 0.20 4
rs6762578
COPG1
3 129273204 intron variant G/A;T snv 2
rs724016
ZBTB38
1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52 5
rs76307059
SMOC2
6 168600208 intron variant C/A;G;T snv 2
rs4073717
FGF18
5 171437017 intron variant G/T snv 0.23 2
rs509035
GHSR
3 172445659 intron variant G/A snv 0.25 2
rs6824748
LCORL
4 17995443 intron variant G/A snv 0.25 2
rs3814333
COLGALT2
1 184037985 upstream gene variant C/T snv 0.29 3
rs2194411 3 185830875 intergenic variant G/A;C snv 2
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 30
rs212526
ECE1
1 21258448 intron variant T/C snv 0.68 2
rs35506085
IGF2 ; INS-IGF2 ; IGF2-AS
11 2144346 intron variant G/A snv 0.17 3
rs6711710
KCNE4
2 223091692 intron variant T/C snv 0.77 2
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs11014285
PRTFDC1
10 24889935 intron variant G/A snv 0.11 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs508347
JAZF1
7 28173205 intron variant T/C snv 0.69 2
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25 4
rs55745410
PHC2
1 33337216 intron variant A/G snv 0.28 2
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 14
rs6899155 5 36786357 intergenic variant T/C snv 0.44 2
rs5750823
TAB1 ; LOC100506472
22 39433968 intron variant C/T snv 0.70 3