Disease: Lean body mass
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 2
rs55745410
PHC2
1 33337216 intron variant A/G snv 0.28 2
rs62372052 5 42724192 upstream gene variant A/G snv 6.9E-02 2
rs724016
ZBTB38
1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52 5
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 30
rs2900208
ETV6
12 11725530 intron variant C/A snv 0.29 2
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs35320790
SALRNA1
14 60642107 intron variant C/A;G snv 2
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs76307059
SMOC2
6 168600208 intron variant C/A;G;T snv 2
rs74494415
GALR1
18 77260182 intron variant C/A;T snv 2
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 23
rs12509014
NUDT6
4 122904764 intron variant C/T snv 0.63 2
rs16942341
ACAN
15 88845674 synonymous variant C/T snv 3.8E-02 6.4E-02 3
rs3814333
COLGALT2
1 184037985 upstream gene variant C/T snv 0.29 3
rs4373984 12 97398809 intergenic variant C/T snv 0.55 2
rs5750823
TAB1 ; LOC100506472
22 39433968 intron variant C/T snv 0.70 3
rs59985551
EFEMP1
2 55879793 intron variant C/T snv 0.21 2
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
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 14
rs28778940
LOC105376157
9 95536070 intergenic variant G/A snv 0.31 2
rs35506085
IGF2 ; INS-IGF2 ; IGF2-AS
11 2144346 intron variant G/A snv 0.17 3
rs509035
GHSR
3 172445659 intron variant G/A snv 0.25 2
rs6824748
LCORL
4 17995443 intron variant G/A snv 0.25 2