Table 3. Example table: description of genetic variants used in the analyses.

SNP	Locus	Chromosome	Locus relative to gene	Risk allele	Source
rs10923931	NOTCH2	1	Intron 5	T	Zeggini et al
rs10490072	BCL11A	2	3′ of gene	T	Zeggini et al
rs7578597	THADA	2	Missense, exon 24	T	Zeggini et al
rs1470579	IGF2BP2	3	Intron 2	C	Saxena et al
rs1801282	PPARg	3	Intron 1	C	Saxena et al
rs4607103	ADAMTS9	3	Intron 2	C	Zeggini et al
rs7754840	CDKAL1	6	Intron 5	C	Saxena et al
rs9472138	VEGFA	6	3′ of gene	T	Zeggini et al
rs864745	JAZF1	7	Intron 1	T	Zeggini et al
rs13266634	SLC30A8	8	Missense, exon 8	C	Saxena et al
rs10811661	CDKNA/2B	9	5′ of gene	T	Saxena et al
rs1111875	HHEX	10	3′ of gene	C	Saxena et al
rs12779790	CDC123,CAMK1D	10	3′ of gene	G	Zeggini et al
rs7903146	TCF7L2	10	Intron 6	T	Saxena et al
rs5219	KCNJ11	11	Missense, exon 1	T	Saxena et al
rs689	INS	11	Intron 1	T	Meigs et al
rs1153188	DCD	12	5′ of gene	A	Zeggini et al
rs7961581	TSPAN8, LGR5	12	5′ of gene	C	Zeggini et al

Adapted from ref. 48.