TABLE 7

Most common haplotypes and frequencies (>5%) in several populations

Nucleotide −1023 −709 −654 −468 −406 −367 −47 −20 46 79 252 491 523 Ca A A As H-L
Alleles G/A C/A G/A C/G C/T T/C T/C T/C G/A C/G G/A C/T C/A
Location 5′ 5′ 5′ 5′ 5′ 5′ 5′LC 5′ Gly16Arg Gln27Glu syn Thr164Ile syn
Haplotype:
1 A C G C C T T T A C G C C 0.7a 25.0a 12.5a 10.0a
2 A C G G C C C C G G G C C 48.3 6.3 10.0 26.7
4 G C A C C T T T A C G C C 33.0 29.7 45.0 40.0
6 G C G C C T T T G C A C A 13.2 31.3 30.0 13.3
  • Nucleotide number is based on the first nucleotide of the start codon being + 1. The frequencies are reported for the indicated populations as follows: Ca, Caucasian; A A, African American; As, Asian; H-L, Hispanic-Latino. Alleles, the two nucleotide possibilities at each SNP position. 5′,5′ upstream of the β2AR open reading frame; 5′LC, 5′ leader cistron; Syn, synonymous SNP. Adapted from Drysdale et al., 2000.

  • a Frequency is shown by percentage.