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rs17616

From SNPedia

Orientationplus
Stabilizedplus
Make rs17616(A;A)
Make rs17616(A;G)
Make rs17616(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position207473578
GeneCR2
is asnp
is mentioned by
dbSNPrs17616
ebirs17616
HLIrs17616
Exacrs17616
Varsomers17616
Maprs17616
PheGenIrs17616
hapmaprs17616
1000 genomesrs17616
hgdprs17616
ensemblrs17616
gopubmedrs17616
geneviewrs17616
scholarrs17616
googlers17616
pharmgkbrs17616
gwascentralrs17616
openSNPrs17616
23andMers17616
23andMe allrs17616
SNP Nexus

SNPshotrs17616
SNPdbers17616
MSV3drs17616
GWAS Ctlgrs17616
GMAF0.2677
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19387458OA-icon.png] Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing


[PMID 17360460OA-icon.png] Association of a common complement receptor 2 haplotype with increased risk of systemic lupus erythematosus.


[PMID 21347408OA-icon.png] Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease.


GET Evidence
CR2-R671H
aa_change Arg671His
aa_change_short R671H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.296875
summary