Product Details

SNP ID
rs6429600
Assay Type
Functionally Tested
NCBI dbSNP Submissions
40
Location
Chr.1:46398839 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGTGAGCCACCACTCCCGGATTCTT[A/G]GCTGTGTCCAAGGAGGACACAGCTG
Phenotype
MIM: 602935
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
FAAH PubMed Links
Additional Information
For this assay, SNP(s) [rs45578535] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
FAAH
Gene Name
fatty acid amide hydrolase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001441.2 Intron NP_001432.2

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