Table 2.

Strongest associations for Age-AR.

SNP ID-Allele	Location	Consequence	Gene	$\beta$-GTxSex	P-GTxSex	Frequency
rs445398-T	9:954,336	intron	DMRT1	5.81	9.8E-9	0.165
rs969092-A	12:42,234,778	intron/NCT	RP11-630C16.2	4.96	8.9E-7	0.238
rs11066997-T	12:114,661,524	intergenic	–	4.94	9.9E-7	0.358
rs11070771-G	15:50,669,890	intergenic	–	−4.86	1.4E-6	0.327
rs4775878-T	15:50,672,420	intergenic	–	−4.86	1.4E-6	0.326
rs12542317-T	8:70,715,243	intron	SLCO5A1	−4.81	1.9E-6	0.326
rs3734266-C	6:34,823,187	intron	UHRF1BP1	4.66	3.9E-6	0.106
rs13130318-G	4:155,538,470	upstream	FGG	4.64	4.2E-6	0.133
rs1397623-T	4:13,887,783	intron/NCT	RP11-341G5.1	−4.60	5.2E-6	0.458
rs7743724-A	6:34,725,478	intron	SNRPC	4.55	6.4E-6	0.101

Shown are the top 10 associated variants. SNP rs ID with the associated allele, physical position in the chromosome, SO consequence type, gene name, effect size of the interaction between genotype and sex ($\beta$_GTxSex) with the corresponding association p-value (P_GTxSex), and the frequency of the associated allele. NCT: noncoding transcript variant.