Table 2.

SNPs Evaluated

Chromosome	SNP number	Position*	Hardy-Weinberg P	% Genotyped	Minor Allele Freq.	Alleles (Common: Minor)
12	rs7975232	48238837	0.78	96.7	0.50	C:A
12	rs2239182	48255411	0.57	94.7	0.49	A:G
12	rs2189480	48263828	0.66	96.2	0.40	C:A
12	rs3819545	48265006	0.10	99.1	0.41	T:C
12	rs3782905	48266167	0.83	99.7	0.30	G:C
12	rs10735810†	48272895	1.00	99.3	0.39	G:A
12	rs2853559	48282805	0.35	95.2	0.36	C:T
12	rs4516035	48299826	0.04	94.3	0.34	T:C
12	rs10877013	58165085	2 × 10−5	97.9	0.39	C:T
4	rs4588 (DBP-2)	72618323	0.72	98.5	0.28	C:A
4	rs7041 (DBP-1)	72618334	0.29	98.6	0.48	T:G
4	rs2298849	72648851	0.01	98.8	0.22	T:C

^*UCSC Genome Browser http://genome.ucsc.edu/build 37.1 (GRCh37), dbSNP build 131 (University of California at Santa Cruz).

^†rs10735810 has been merged into rs2228570 at the same position with alleles C and T (http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene; National Institutes of Health, Bethesda, MD).