rs4308977

Orientation

plus

Stabilized

plus

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

Make rs4308977(C;C)

Make rs4308977(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

207473553

Gene

CR2

is a	snp
is	mentioned by
dbSNP	rs4308977
dbSNP (classic)	rs4308977
ClinGen	rs4308977
ebi	rs4308977
HLI	rs4308977
Exac	rs4308977
Gnomad	rs4308977
Varsome	rs4308977
LitVar	rs4308977
Map	rs4308977
PheGenI	rs4308977
Biobank	rs4308977
1000 genomes	rs4308977
hgdp	rs4308977
ensembl	rs4308977
geneview	rs4308977
scholar	rs4308977
google	rs4308977
pharmgkb	rs4308977
gwascentral	rs4308977
openSNP	rs4308977
23andMe	rs4308977
SNPshot	rs4308977
SNPdbe	rs4308977
MSV3d	rs4308977
GWAS Ctlg	rs4308977

GMAF

0.2975

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

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

ClinVar
Risk	rs4308977(A;A) rs4308977(C;C)
Alt	rs4308977(A;A) rs4308977(C;C)
Reference	Rs4308977(T;T)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	CR2
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.207646898T>C
CLNSRC
CLNACC	RCV000455766.1,