Disease: Lean body mass
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2194411 3 185830875 intergenic variant G/A;C snv 2
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 23
rs35320790
SALRNA1
14 60642107 intron variant C/A;G snv 2
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 7
rs6762578
COPG1
3 129273204 intron variant G/A;T snv 2
rs74494415
GALR1
18 77260182 intron variant C/A;T snv 2
rs76307059
SMOC2
6 168600208 intron variant C/A;G;T snv 2
rs147110934
ZNF628
19 55482069 missense variant G/T snv 1.4E-02 1.5E-02 3
rs7952436
KDM2A
11 67257063 3 prime UTR variant C/T snv 4.7E-02 3
rs16942341
ACAN
15 88845674 synonymous variant C/T snv 3.8E-02 6.4E-02 3
rs62372052 5 42724192 upstream gene variant A/G snv 6.9E-02 2
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs72656010
PLAG1 ; CHCHD7
8 56209656 intron variant T/C snv 0.10 3
rs11014285
PRTFDC1
10 24889935 intron variant G/A snv 0.11 2
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs35506085
IGF2 ; INS-IGF2 ; IGF2-AS
11 2144346 intron variant G/A snv 0.17 3
rs4870941 8 125486586 intron variant G/C snv 0.20 4
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 10
rs59985551
EFEMP1
2 55879793 intron variant C/T snv 0.21 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