rs398122863

Orientation

plus

Stabilized

plus

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

Make rs398122863(A;A)

Make rs398122863(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

207474297

Gene

CR2

is a	snp
is	mentioned by
dbSNP	rs398122863
dbSNP (classic)	rs398122863
ClinGen	rs398122863
ebi	rs398122863
HLI	rs398122863
Exac	rs398122863
Gnomad	rs398122863
Varsome	rs398122863
LitVar	rs398122863
Map	rs398122863
PheGenI	rs398122863
Biobank	rs398122863
1000 genomes	rs398122863
hgdp	rs398122863
ensembl	rs398122863
geneview	rs398122863
scholar	rs398122863
google	rs398122863
pharmgkb	rs398122863
gwascentral	rs398122863
openSNP	rs398122863
23andMe	rs398122863
SNPshot	rs398122863
SNPdbe	rs398122863
MSV3d	rs398122863
GWAS Ctlg	rs398122863

Max Magnitude

0

ClinVar
Risk	rs398122863(A;A)
Alt	rs398122863(A;A)
Reference	Rs398122863(G;G)
Significance	Pathogenic
Disease	Common variable immunodeficiency 7
Variation	info
Gene	CR2
CLNDBN	Common variable immunodeficiency 7
Reversed	0
HGVS	NC_000001.10:g.207647642G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000029132.24,