Two Rare Variants Explain Association with Acute Myocardial Infarction in an Extended Genomic Region Including the Apolipoprotein(A) Gene
Version of Record online: 21 DEC 2012
© 2012 Blackwell Publishing Ltd/University College London
Annals of Human Genetics
Volume 77, Issue 1, pages 47–55, January 2013
How to Cite
Koch, W., Mueller, J. C., Schrempf, M., Wolferstetter, H., Kirchhofer, J., Schömig, A. and Kastrati, A. (2013), Two Rare Variants Explain Association with Acute Myocardial Infarction in an Extended Genomic Region Including the Apolipoprotein(A) Gene. Annals of Human Genetics, 77: 47–55. doi: 10.1111/j.1469-1809.2012.00739.x
- Issue online: 21 DEC 2012
- Version of Record online: 21 DEC 2012
- Manuscript Accepted: 2 OCT 2012
- Manuscript Received: 23 MAY 2012
Additional Supporting Information may be found in the online version of this article.
Table S1 Oligonucleotide primers and TaqMan probes used for genotyping.
Table S2 Genotype distributions in the AMI group and control group.
Figure S1 Linkage disequilibrium in the SLC22A3-LPAL2-LPA region and positions of SNPs selected for a haplotype analysis.
Figure S2 Linkage disequilibrium between SNPs shown as D’ values.
Figure S3 Linkage disequilibrium between SNPs shown as r2 values.
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