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Rs1801133
CHF 39.40
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SKU
H37HV7U6ID7
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Geliefert zwischen Do., 26.02.2026 und Fr., 27.02.2026
Details
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. C677T or rs1801133 is a genetic variation a single nucleotide polymorphism (SNP) in the MTHFR gene. Among Americans the frequency of T-homezygosity ranges from 1% or less among Blacks to 20% or more among Italiens and Hispanics. In 2000 association studies on oral clefts, Down syndrome, and fetal anticonvulsant syndrome were either unreplicated or had yielded conflicting results. A single-nucleotide polymorphism (SNP, pronounced snip) is a DNA sequence variation occurring when a single nucleotide A, T, C, or G in the genome (or other shared sequence) differs between members of a species (or between paired chromosomes in an individual). For example, two sequenced DNA fragments from different individuals, AAGCCTA to AAGCTTA, contain a difference in a single nucleotide. In this case we say that there are two alleles : C and T. Almost all common SNPs have only two alleles.
Weitere Informationen
- Allgemeine Informationen
- GTIN 09786130592974
- Editor Lambert M. Surhone, Miriam T. Timpledon, Susan F. Marseken
- Größe H220mm x B220mm
- EAN 9786130592974
- Format Fachbuch
- Titel Rs1801133
- Herausgeber Betascript Publishing
- Anzahl Seiten 108
- Genre Biologie
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