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
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
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs4755720
HSD17B12
11 43607199 intron variant C/T snv 0.60 2