Table 1.

Information on ten genotyped tagging single‐nucleotide polymorphisms (tSNPs) of the Runt‐related transcription factor 3 (RUNX3) gene

SNP no.	NCBI reference SNP no.	Chromosome position †	Location	Base change	MAF			P *	P for HWE**
					Database ‡	Cases	Controls
1	rs6672420	25163597	Exon 1	T   A	0.289	0.314	0.288	0.329	0.268
2	rs11249208	25155713	Intron 1	A   G	0.330	0.267	0.255	0.332	0.129
3	rs11249206	25150569	Intron 1	T   C	0.378	0.466	0.387	0.005	0.388
4	rs7551188	25145787	Intron 1	T   C	0.489	0.407	0.433	0.364	0.501
5	rs1395621	25143159	Intron 1	C   T	0.411	0.420	0.426	0.865	0.147
6	rs906296	25137245	Intron 1	G   C	0.256	0.250	0.263	0.608	0.152
7	rs760805	25124510	Intron 3	T   A	0.464	0.393	0.467	0.008	0.306
8	rs2236852	25116354	Intron 4	A   G	0.477	0.434	0.472	0.177	0.067
9	rs9438876	25113703	Intron 4	A   G	0.244	0.285	0.289	0.902	0.514
10	rs2282718	25113643	Intron 4	G   A	0.333	0.383	0.382	1.000	0.296

^† SNP position in NCBI dbSNP (http://www.ncbi.nlm.nih.gov/projects/SNP).

^‡ Minor allele frequency (MAF) for Han Chinese in Beijing in the HapMap database (http://www.hapmap.org).

^* P‐value for the allele distribution difference between the cases and controls.

^** Hardy–Weinberg equilibrium (HWE) P‐value in the control group.