Disease: Age at menarche
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs707938
MSH5-SAPCD1 ; MSH5 ; SAPCD1
6 31761582 synonymous variant A/G snv 0.38 0.44 3
rs11209943
LOC105378797
1 72284817 intron variant A/G snv 0.53 2
rs13064915 3 137402401 intergenic variant T/C snv 0.42 2
rs80170948
SREK1IP1
5 64724489 missense variant T/G snv 3.0E-02 2.8E-02 2