Table 1. Index SNPs (P_emmax ≤ 5 × 10⁻⁶, at least one supporting SNP in LD with R² > 0.6) for candidate associated regions.

RSID	CHR	POSITION Assembly 3GRCh37.p13	ALLELES (effect allele bold)	Freq EA	Type	P	OR*,**	Within gene
rs116828186	3	18854524	A,G	0.027	Genotyped	1.37E-06	0.824	—
rs28731189	5	11212170	C,T	0.011	Imputed	1.42E-06	0.736	CTNND2
rs74291850	5	29577370	T,C	0.022	Imputed	4.63E-07	1.291	—
rs187984259	5	73681906	T,C	0.016	Imputed	1.43E-06	0.758	—
rs80317841	6	132398394	G,C	0.84	Genotyped	1.97E-06	1.092	—
rs116141145	7	97249265	A,G	0.037	Imputed	1.24E-06	1.190	—
rs111513399	8	69036056	A,G	0.113	Imputed	5.38E-07	1.114	PREX2
rs11258313	10	13339766	G,A	0.233	Imputed	1.35E-06	1.101	PHYH
rs12774519	10	18925493	C,G	0.191	Imputed	2.06E-06	1.086	NSUN6
rs9895748	17	5053598	T,A	0.068	Imputed	1.72E-06	0.872	USP6
rs62079945	18	10247566	A,C	0.048	Imputed	1.22E-06	0.842	—
rs6033064	20	1175527	T,C	0.803	Imputed	9.94E-07	0.909	—

^*Expected frequency of the effect allele.

^**The OR indicates the estimated allele frequency odds ratio for the effect allele. Values less than one indicate that the effect allele is less common in cases than controls and vice versa.