Disease: Body Fat Distribution
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 13
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 8
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 7
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 7
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs62621197
ADAMTS10
1.000 0.080 19 8605262 missense variant C/A;T snv 4.1E-06; 3.1E-02 2.9E-02 4
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 3
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 3
rs3817428
ACAN
15 88872016 missense variant C/G snv 0.20 0.20 3
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 3
rs17511102
LOC105374465 ; CDC42EP3
2 37733470 intron variant A/G;T snv 2
rs28584580
ACAN
15 88854596 intron variant A/G snv 0.11 2
rs35344761
PCSK5
9 75895907 intron variant C/A snv 0.10 2
rs4694504 4 72630974 intergenic variant A/G;T snv 2
rs798491
AMZ1 ; GNA12
7 2760887 intron variant A/C;G snv 2
rs991967
TGFB2-OT1 ; TGFB2
1 218442109 3 prime UTR variant A/C snv 0.37 2
rs994014 4 81244636 intergenic variant T/C snv 0.43 2