Disease: Lean body mass
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 30
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 23
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 14
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 10
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 7
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs724016
ZBTB38
1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52 5
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs4870941 8 125486586 intron variant G/C snv 0.20 4
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25 4
rs147110934
ZNF628
19 55482069 missense variant G/T snv 1.4E-02 1.5E-02 3
rs16942341
ACAN
15 88845674 synonymous variant C/T snv 3.8E-02 6.4E-02 3
rs35506085
IGF2 ; INS-IGF2 ; IGF2-AS
11 2144346 intron variant G/A snv 0.17 3
rs3814333
COLGALT2
1 184037985 upstream gene variant C/T snv 0.29 3
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs5750823
TAB1 ; LOC100506472
22 39433968 intron variant C/T snv 0.70 3
rs72656010
PLAG1 ; CHCHD7
8 56209656 intron variant T/C snv 0.10 3
rs7952436
KDM2A
11 67257063 3 prime UTR variant C/T snv 4.7E-02 3
rs11014285
PRTFDC1
10 24889935 intron variant G/A snv 0.11 2
rs12509014
NUDT6
4 122904764 intron variant C/T snv 0.63 2
rs212526
ECE1
1 21258448 intron variant T/C snv 0.68 2
rs2194411 3 185830875 intergenic variant G/A;C snv 2