Table 1.

SNPs in identified risk locus

rsID	Chr	Position	Ref	Alt	Gnomad MAF (EUR)	P-value	nCand. SNPs
rs12465214	2	185198135	C	A	0.45	5.78E−15	160
rs2219224	2	185211739	G	A	0.52	1.03E−09	41
rs17582219	2	184983620	A	G	0.34	3.70E−09	40
rs7593266	2	184965195	T	G	0.45	2.40E−08	149
rs12621296	2	185099836	A	G	0.62	3.27E−08	131

Chr, chromosome; EUR, European (non-Finnish); MAF, minor allele frequency; nCand. SNPs, the number of unique candidate SNPs in the genomic locus.