Disease: Age at menarche
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 4
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs4929923
TRIM66
11 8617653 3 prime UTR variant T/C snv 0.59 3
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 3