Product Details

SNP ID
rs17044576
Assay Type
Functionally Tested
NCBI dbSNP Submissions
53
Location
Chr.1:207461325 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AACCACTAATTTTTACTTGTAAGGG[C/T]GAAGGAGATGGAACAATTCTGAGGA
Phenotype
MIM: 120650
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CR2 PubMed Links
Additional Information
For this assay, SNP(s) [rs74857976] 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
CR2
Gene Name
complement component 3d receptor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001006658.2 Intron NP_001006659.1
NM_001877.4 Intron NP_001868.2
XM_011509206.2 Intron XP_011507508.1

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