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bn:01123224n
Noun Named Entity
Categories: SNPs on chromosome 1
EN
rs1801133  C677T
EN
C677T or rs1801133 is a genetic variation—a single nucleotide polymorphism —in the MTHFR gene. Wikipedia
Definitions
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Sources
EN
C677T or rs1801133 is a genetic variation—a single nucleotide polymorphism —in the MTHFR gene. Wikipedia
Genetic variation—single nucleotide polymorphism (SNP)—in the MTHFR gene Wikidata
IS A
single nucleotide polymorphism
PART OF
methylenetetrahydrofolate reductase
CHROMOSOME
chromosome 1
GENETIC ASSOCIATION
cardiovascular disease
spontaneous abortion
hyperhomocysteinemia
Wikipedia
EN
rs1801133
Wikidata
EN
rs1801133
Wikipedia Redirections
EN
C677T
Wikidata Alias
EN
C677T

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