Disease: Hip circumference
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs10929925 2 6015425 intergenic variant C/A;T snv 3
rs1808579
RMC1 ; NPC1
18 23524924 intron variant C/T snv 0.47 3
rs3888190
ATP2A1
16 28878165 upstream gene variant C/A;T snv 0.35 3