Disease: Age at menarche
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
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
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7