rs17615

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs17615(A;A)

Make rs17615(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

207473117

Gene

CR2

is a	snp
is	mentioned by
dbSNP	rs17615
dbSNP (classic)	rs17615
ClinGen	rs17615
ebi	rs17615
HLI	rs17615
Exac	rs17615
Gnomad	rs17615
Varsome	rs17615
LitVar	rs17615
Map	rs17615
PheGenI	rs17615
Biobank	rs17615
1000 genomes	rs17615
hgdp	rs17615
ensembl	rs17615
geneview	rs17615
scholar	rs17615
google	rs17615
pharmgkb	rs17615
gwascentral	rs17615
openSNP	rs17615
23andMe	rs17615
SNPshot	rs17615
SNPdbe	rs17615
MSV3d	rs17615
GWAS Ctlg	rs17615

GMAF

0.2686

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 19387458] Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing

OMIM	120650
Desc	COMPLEMENT COMPONENT RECEPTOR 2; CR2
Variant
Related	also

OMIM	120650
Desc
Variant	0001
Related	also

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

[PMID 27446959] 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,