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(Q4048578)

English

rs1801133

genetic variation—single nucleotide polymorphism (SNP)—in the MTHFR gene

C677T

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Statements

single-nucleotide polymorphism

0 references

1 reference

Concept mapping One-Carbon Metabolism to model future ontologies for nutrient-gene-phenotype interactions

genetic association

cardiovascular disease

1 reference

Concept mapping One-Carbon Metabolism to model future ontologies for nutrient-gene-phenotype interactions

1 reference

Concept mapping One-Carbon Metabolism to model future ontologies for nutrient-gene-phenotype interactions

hyperhomocysteinemia

1 reference

Concept mapping One-Carbon Metabolism to model future ontologies for nutrient-gene-phenotype interactions

human chromosome 1

genomic assembly

genome assembly GRCh38

0 references

11796321

genomic assembly

genome assembly GRCh38

0 references

11796321

genomic assembly

genome assembly GRCh38

0 references

Identifiers

dbSNP Reference SNP number

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0 references

HGVS nomenclature

chr1:g.11856378G>A

genomic assembly

Genome assembly GRCh37

1 reference

https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=1801133

NC_000001.11:g.11796321G>A

genomic assembly

genome assembly GRCh38

1 reference

https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=1801133

Sitelinks

Wikipedia(2 entries)

enwiki Rs1801133
ruwiki Rs1801133

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