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rs398122863

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122863(A;A)
Make rs398122863(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position207474297
GeneCR2
is asnp
is mentioned by
dbSNPrs398122863
ebirs398122863
HLIrs398122863
Exacrs398122863
Varsomers398122863
Maprs398122863
PheGenIrs398122863
hapmaprs398122863
1000 genomesrs398122863
hgdprs398122863
ensemblrs398122863
gopubmedrs398122863
geneviewrs398122863
scholarrs398122863
googlers398122863
pharmgkbrs398122863
gwascentralrs398122863
openSNPrs398122863
23andMers398122863
23andMe allrs398122863
SNP Nexus

SNPshotrs398122863
SNPdbers398122863
MSV3drs398122863
GWAS Ctlgrs398122863
Max Magnitude0
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,