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SNP ID:
rs1876453
Gene
CR2
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.1: 207454573 - 207454573 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

AGCAGGGGGCCAAAAGCGAGACGGT[A/G]GGGGCAGTGCTCGACGCGTGTCCGC

Assay ID C__12082991_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 23 submissions

Phenotype:

 MIM: 120650

Literature Links:

 CR2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.05)
(0.95)
Caucasian
A (0.13)
(0.87)
CEPH (CEU) - Not Available
EAS
A (0.00)
(1.00)
African American
A (0.10)
(0.90)
YRI (Yoruba)
A (0.03)
(0.97)
SAS
A (0.04)
(0.96)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
A (0.07)
(0.93)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
A (0.09)
(0.91)
AMR
A (0.04)
(0.96)
CR2 - complement component 3d receptor 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid 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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