Disease: Lean body mass
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11014285
PRTFDC1
10 24889935 intron variant G/A snv 0.11 2
rs12509014
NUDT6
4 122904764 intron variant C/T snv 0.63 2
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
rs212526
ECE1
1 21258448 intron variant T/C snv 0.68 2
rs2194411 3 185830875 intergenic variant G/A;C snv 2
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs28778940
LOC105376157
9 95536070 intergenic variant G/A snv 0.31 2
rs2900208
ETV6
12 11725530 intron variant C/A snv 0.29 2
rs35320790
SALRNA1
14 60642107 intron variant C/A;G snv 2
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
rs4073717
FGF18
5 171437017 intron variant G/T snv 0.23 2
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs4373984 12 97398809 intergenic variant C/T snv 0.55 2
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs4870941 8 125486586 intron variant G/C snv 0.20 4
rs508347
JAZF1
7 28173205 intron variant T/C snv 0.69 2
rs509035
GHSR
3 172445659 intron variant G/A snv 0.25 2
rs55745410
PHC2
1 33337216 intron variant A/G snv 0.28 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
rs62372052 5 42724192 upstream gene variant A/G snv 6.9E-02 2
rs6711710
KCNE4
2 223091692 intron variant T/C snv 0.77 2