Product Details

SNP ID: rs1255396
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.10:42543739 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: AATGGAATAGGTAATTCCAAAATTC[T/C]ATCCCAAACTAAAGCAACAATTAAG
Phenotype
Polymorphism: T/C, Transition Substitution
Allele Nomenclature
Literature Links: ZNF37BP PubMed Links
Additional Information: For this assay, SNP(s) [rs73262610] 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

There are no transcripts associated with this gene.