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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