Association of ADAMTS13 polymorphism with cerebral malaria

Malaria Journal

Table 1 SNPs analysed in this study

rs#^a	HGVS name^{a, b}	Chromosome coordinate^a	Region^a	Ancestral allele/derived allele^a (Allele frequency^c)
rs2301611	g.8488T >C	136290607	intron 3	T (0.854)/C (0.146)
rs3118667	g.8944C >T	136291063	exon 5	T (0.803)/C (0.197)
rs739469	g.16610G >C	136298729	intron 10	C (0.213)/G (0.787)
rs652600	g.28898G >A	136311017	intron 20	T (0.247)/C (0.753)
rs4962153	g.41635A >G	136323754	intron 28	G (0.921)/A (0.079)
rs1055432	g.42120C >A	136324239	exon 29	C (0.750^d)/A (0.250)

Note; HGVS (Human Genome Variation Society) name
^a The SNP reference number, HGVS name, chromosome coordinate, region, and ancestral state were retrieved from the National Center for Biotechnology Information (NCBI) SNP database build 132, September 2010.
^b The position of SNP was determined according to the HGVS nomenclature based on the NCBI reference sequence NG_011934.1.
^c The allele frequency in the Asian HapMap populations (JPT+CHB).
^d The Asian HapMap samples were genotyped in this study.

ISSN: 1475-2875