. Author manuscript; available in PMC: 2017 Aug 29.

Published in final edited form as: Hum Genet. 2010 Jan 19;127(5):503–512. doi: 10.1007/s00439-010-0787-6

Table 3.

Probability (p) values for risk alleles significantly associated with at least one ND measure under the additive model in pooled, European-American, and African-American samples

dbSNP ID	Risk/minor allele	Pooled sample				European-American sample				African-American sample

		MAF	SQ	HSI	FTND	MAF	SQ	HSI	FTND	MAF	SQ	HSI	FTND
rs7030238	C/C	0.286	0.0030	0.0033	0.0044	0.226	0.1047	0.0873	0.2407	0.317	0.0145	0.0163	0.0100
rs10512282	G/G	0.082	0.0256	0.0500	0.0683	0.091	0.0456	0.0419	0.0549	0.078	0.2055	0.349	0.3965
rs11788456	G/G	0.451	0.0674	0.2436	0.1963	0.455	0.0016	0.0102	0.0014	0.449	0.8465	0.869	0.690
rs17189632	T/A	0.389	0.0003	0.0003	0.0002	0.446	0.0042	0.0094	0.0129	0.359	0.0103	0.0071	0.0037
rs10121600	C/^a	0.481 (T)	0.0005	0.0032	0.0050	0.358 (T)	0.0039	0.0367	0.0383	0.454 (C)	0.0218	0.0288	0.0428
rs1924032	A/G	0.491	0.0435	0.1164	0.1270	0.498	0.4877	0.8943	0.6218	0.486	0.0477	0.0889	0.1495
rs2067056	C/^a	0.418 (C)	0.0911	0.3091	0.2883	0.496 (T)	0.0236	0.1401	0.0561	0.372 (C)	0.5822	0.7873	0.9348

The p values that remained significant after correction for multiple testing are shown in bold. The adjusted p values for multiple testing at the 0.05 significance level based on the SNPSpD program are 0.0037, 0.0034, and 0.0045, respectively, for the pooled, EA, and AA samples MAF minor allele frequency; SQ number of cigarettes smoked per day; HSI heaviness of smoking index (0–6 point scale); FTND Fagerström test for ND score (0–10 point scale)

Minor allele differs among samples and is given individually for each sample