Table 1.
Allele frequencies of SNPs in putative N-6 adenine-specific DNA methyltransferase 1 (N6AMT1).
| SNPb | SNP typeb | Basec | Positionb | n | Andean study population | HapMap allele frequenciesa (%) | ||
|---|---|---|---|---|---|---|---|---|
| Allele frequency (%)d | European | Asian | African | |||||
| rs1997605 | Intron 1 | A/G | 30257418 | 188 | 53/47 | 85/15 | 50/50 | 65/35 |
| rs2205449 | Intron 4 | A/T | 30252088 | 188 | 38/63 | 59/41 | 25/75 | 18/82 |
| rs2705671 | Intron 4 | T/G | 30251349 | 184 | 58/42 | 86/14 | 69/31 | 94/6 |
| rs16983411 | Intron 5 | A/G | 30250247 | 185 | 99/1 | 84/16 | 87/13 | 82/18 |
| rs1048546 | 3´UTR | G/T | 30244877 | 187 | 53/47 | 69/31 | 37/63 | 59/41 |
| aAllele frequencies for Europeans, Asians, and Africans from HapMap CEU (CEPH, Utah residents with ancestry from northern and western Europe), JPT (Japanese in Tokyo, Japan), and YRI (Yoruba in Ibadan, Nigeria), respectively (Thorisson etal. 2005). bFrom the NCBI dbSNP Single Nucleotide Polymorphisms database (http://www.ncbi.nlm.nih.gov/SNP), genome build 37.3. cAlleles associated with lower %MMA are denoted first. dChi-square values from the test of Hardy Weinberg equilibrium were 2.73 for rs1997605, 0.41 for rs2205449, 3.21 for rs2705671, <0.001 for rs16983411, and 2.11 for rs1048546. | ||||||||