Table I.
rs# | SNP location | Base pair change (major > minor) | Minor allele frequencya |
rs4253730 | Intron 3 | A > G | 0.182 |
rs4253760b | Intron 6 | T > G | 0.196 |
rs4253705 | Intron 2 | T > C | 0.190 |
rs135543 | Intron 2 | G > A | 0.283 |
rs135542b | Intron 2 | A > G | 0.205 |
rs4253649 | Not validated | C > G | 0.370 |
rs4253758 | Intron 6 | T > C | 0.217 |
rs4253699b | Intron 2 | T > C | 0.182 |
rs4253655 | Intron 2 | G > A | 0.143 |
rs4253681 | Intron 2 | T > C | 0.136 |
rs4253755b | Intron 5 | G > A | 0.130 |
rs4253706 | Intron 2 | G > A | 0.119 |
rs4253623b | Intron 2 | A > G | 0.109 |
rs1800206b | Exon 5 Leu > Val | C > G | 0.022 |
Sequence data on 23 European American Coriell samples are available on the University of Washington-Fred Hutchinson Center Research Center Variation Discovery Resource (PGA) website (http://pga.gs.washington.edu/).
SNPs included in analyses.