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rs17615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17615(A;A)
Make rs17615(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position207473117
GeneCR2
is asnp
is mentioned by
dbSNPrs17615
dbSNP (old)rs17615
ClinGenrs17615
ebirs17615
HLIrs17615
Exacrs17615
Gnomadrs17615
Varsomers17615
Maprs17615
PheGenIrs17615
Biobankrs17615
1000 genomesrs17615
hgdprs17615
ensemblrs17615
gopubmedrs17615
geneviewrs17615
scholarrs17615
googlers17615
pharmgkbrs17615
gwascentralrs17615
openSNPrs17615
23andMers17615
23andMe allrs17615
SNPshotrs17615
SNPdbers17615
MSV3drs17615
GWAS Ctlgrs17615
GMAF0.2686
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 19387458OA-icon.png] Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing

OMIM120650
DescCOMPLEMENT COMPONENT RECEPTOR 2; CR2
Variant
Relatedalso
OMIM120650
Desc
Variant0001
Relatedalso


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



[PMID 27446959OA-icon.png] Association of Complement Receptor 2 Gene Polymorphisms with Susceptibility to Osteonecrosis of the Femoral Head in Systemic Lupus Erythematosus.


ClinVar
Risk rs17615(A;A)
Alt rs17615(A;A)
Reference Rs17615(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CR2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.207646462G>A
CLNSRC
CLNACC RCV000455065.1,