Table 1.

Significant SNPs in Chr8p21.3 next to GFRA2

Chr	SNP	Position	Gene	Minor allele	Allele frequency in cases (%)	Allele frequency in controls (%)	p‐value	OR	Information about the SNP
8	rs4872521	21707713	Intergenic	G	21.53	28.82	5.40 × 10−7	0.68	Imputed
8	rs4872522	21707844	Intergenic	C	21.53	28.78	6.47 × 10−7	0.68	Imputed
8	rs10098807	21708824	Intergenic	A	21.63	28.84	7.00 × 10−7	0.68	Imputed
8	rs11774105	21710146	Intergenic	C	21.72	29.06	4.03 × 10−7	0.68	Imputed
8	rs17428041	21711431	Intergenic	C	21.53	29.08	1.77 × 10−7	0.67	In the Illumina OmniExpress
8	rs17615364	21711580	Intergenic	A	21.58	29.08	2.20 × 10−7	0.67	Imputed
8	rs11776842	21711651	Intergenic	C	21.58	29.08	2.20 × 10−7	0.67	Imputed
8	rs12545534	21712401	Intergenic	A	21.58	29.02	2.62 × 10−7	0.67	In the Illumina OmniExpress
8	rs11780601	21717841	Intergenic	T	18.79	25.63	7.98 × 10−7	0.67	In the Illumina OmniExpress

p‐values and ORs were calculated using Fisher's exact test. Chr, chromosome; SNP, single nucleotide polymorphisms; OR, odds ratio.