GG, CC and GC genotypes in the samples.

<p>Fig. 2 A, B and C show GG, CC and GC genotype respectively as shown by the results obtained by RT-PCR.</p

Genotype/allele frequency of SREBF-1(rs2297508) in EC patients and normal controls.

<p>OR odds ratio Cl confidence limit.</p

Genotypic and allelic frequencies of the 10 SNPs in the 6 controls and 30 EC patients.

<p>Genotypic and allelic frequencies of the 10 SNPs in the 6 controls and 30 EC patients.</p

Figure 1

<p>A: SNPs in SREBF-1 gene. The whole SREBF-1gene includes 22 exons. Ten SNPs (SNP1 to SNP10) were identified within the SREBF-1 in our study. FIG. 1 B: SNP ID. SNP1 to SNP10 are listed from 5′-3′ of the SREBF-1. “CHR-ID” shows chromosome ID of ten SNPs in SREBF-1. Listed “RS ID” has been reported in ucsc or NCBI website, “-” expresses newly detected SNP. “Function” column listed altered genetically coded function of the SNPs. “Ref SNP” shows SNP form in original reference sequence. In “mRNA location”, corresponding mRNA positions are showed in consistent with each SNP. (For details:Sequence IDs included in CCDS 32583.1). NCBI db is available from <a href="http://www.ncbi.nlm.nih.gov/SNP" target="_blank">http://www.ncbi.nlm.nih.gov/SNP</a>.</p

Genotype/allele distribution of SREBF-1(rs2297508) in EC patients with different characteristics.

<p>Statistical analysis:Pearson χ2 test.</p><p>Age ≤50 years old, endometrioid type, low grade, stage I and myometrial invasion <1/2 were considered as references for comparison.</p>a<p>Odds ratio(OR) of the GC/CC against the GG genotypes.</p>b<p>Odds ratio(OR) of the C against the G alleles.</p>c<p>Comparison between stage I and II.</p>d<p>Comparison between stage I and III–IV.</p