Product Details

SNP ID: rs168922
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.16:55726426 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTTCCAGCAGCCCACCTCTAGCTGC[C/T]TTCTTTTCTTTCCTTTTTTAAAAAA
Phenotype
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: CES1P2 PubMed Links
Additional Information: For this assay, SNP(s) [rs115506587] are located under a probe 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

There are no transcripts associated with this gene.