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. Author manuscript; available in PMC: 2010 Nov 1.
Published in final edited form as: Hum Genet. 2009 Jul 3;126(5):643–653. doi: 10.1007/s00439-009-0713-y

Table 2.

NOS2A single marker association in African-Americans

Rs # SNP Typea Allele Frequency
(Allele)
OR 95% CI Uncorrected
p valueb
rs8073782 Promoter 0.80(C) / 0.20(T) 0.91 0.65 1.27 0.57
rs61589465 (T-5937C) Promoter 0.96(A) / 0.04(G) 2.15 0.87 5.30 0.10
rs57234985 (T-5091C) Promoter 0.96(A) / 0.04(G) 0.44 0.22 0.91 0.03
rs28998790 (G-1459A) Promoter 0.93(G) / 0.07(A) 1.16 0.53 2.52 0.72
rs57161411 (A-1641C) Promoter 0.99(A) / 0.01(C) 0.67 0.20 2.18 0.50
rs9282799 Promoter 0.94(G) / 0.06(A) 0.96 0.48 1.93 0.91
rs2779248 Promoter 0.53(T) / 0.47(C) 1.03 0.78 1.37 0.83
rs10459953 5′UTR 0.70 (G) / 0.30(C) 0.91 0.66 1.27 0.58
rs2072324 Intron 0.88(C) / 0.12(A) 0.93 0.56 1.55 0.79
rs8072199 Intron 0.82(C) / 0.18(T) 1.29 0.88 1.89 0.20
rs3794764 Intron 0.71(G) / 0.29(A) 0.74 0.52 1.05 0.09
rs17722851 Intron 0.96(T) / 0.04(A) 1.34 0.45 3.99 0.60
rs2314812 Intron 0.84(C) / 0.16(T) 1.00 0.67 1.50 0.99
rs944725 Intron 0.51(C) / 0.49(T) 0.78 0.57 1.08 0.13
rs3730017 Coding Exon (R/W 221) 0.76(G) / 0.24(A) 1.20 0.84 1.70 0.32
rs3729508 Intron 0.83(C) / 0.17(T) 1.76 1.16 2.67 0.01
rs1113283 Intron 0.84(C) / 0.16(T) 0.99 0.66 1.48 0.95
rs9904158 Intron 0.94(G) / 0.06(C) 1.23 0.60 2.54 0.57
rs4795067 Intron 0.82(A) / 0.18(G) 1.14 0.76 1.71 0.52
rs1137933 Coding Exon (D/D 346) 0.85(G) / 0.15(A) 1.00 0.66 1.52 1.00
rs12944039 Intron 0.76(G) / 0.24(A) 0.75 0.53 1.08 0.12
rs16966545 Intron 0.83(T) / 0.17(A) 0.84 0.55 1.31 0.45
rs2314810 Intron 0.99(G) / 0.01(C) 5.71 0.81 40.27 0.08
rs17718148 Intron 0.88(C) / 0.12(T) 1.03 0.64 1.68 0.89
rs3729966 Intron (boundary) 0.86(C) / 0.14(T) 0.75 0.48 1.18 0.22
rs2248814 Intron (boundary) 0.83(G) / 0.17(A) 1.68 1.13 2.50 0.01
rs3729718 Intron (boundary) 0.94(T) / 0.06(G) 0.48 0.28 0.85 0.01
rs2274894 Intron 0.83(G) / 0.17(T) 1.84 1.23 2.77 0.003
rs9797244 Intron 0.83(T) / 0.17(C) 0.92 0.63 1.36 0.68
rs2297518 Coding Exon (S/L 569) 0.89(G) / 0.11(A) 1.17 0.72 1.91 0.51
rs2297516 Intron 0.66(A) / 0.34(C) 0.77 0.54 1.09 0.15
rs2314809 Intron 0.57(T) / 0.43(C) 1.40 1.03 1.92 0.03
rs2297515 Intron 0.97(A) / 0.03(C) 1.80 0.64 5.05 0.27
rs944722 Intron 0.79(T) / 0.21(C) 1.63 1.14 2.33 0.01
rs2255929 Intron 0.57(A) / 0.43(T) 1.45 1.06 1.99 0.02
rs3794756 Intron 0.91(C) / 0.09(T) 0.71 0.42 1.18 0.19
rs11653716 Intron 0.66(C) / 0.34(G) 1.01 0.73 1.42 0.93
rs7406657 Downstream 0.82(G) / 0.18(C) 0.90 0.61 1.32 0.59
rs7215373 Downstream 0.76(C) / 0.24(T) 1.67 1.17 2.37 0.004

Statistically significant p values (p<0.05) are in bold; an allele frequencies are for founders; and all analyses were adjusted for age (years) and gender

a

SNPs type was determined using SNPper software available from http://snpper.chip.org

b

These p values are uncorrected for multiple comparisons