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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Association of MTHFD1 G1958A (rs2236225) gene polymorphism with the risk of congenital heart disease: a systematic review and meta-analysis

Fig. 1

The location of G1958A (rs2236225) polymorphism in MTHFD1 gene (SNP2). The genetic variation is named according to the DNA sequence of the human MTHFD1 gene (Genbank database: NG_011992). The transcription start site is located at 1350 in the promoter. Figure 1 is drawn by Illustrator for Biological Sequences (IBS 2.0). Abbreviations: transcriptional start sites (TSS); coding DNA sequences (CDS); single nucleotide polymorphism (SNP)

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BMC Medical Genomics

ISSN: 1755-8794

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