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rs398122864

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122864(C;C)
Make rs398122864(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position207470103
GeneCR2
is asnp
is mentioned by
dbSNPrs398122864
ebirs398122864
HLIrs398122864
Exacrs398122864
Varsomers398122864
Maprs398122864
PheGenIrs398122864
hapmaprs398122864
1000 genomesrs398122864
hgdprs398122864
ensemblrs398122864
gopubmedrs398122864
geneviewrs398122864
scholarrs398122864
googlers398122864
pharmgkbrs398122864
gwascentralrs398122864
openSNPrs398122864
23andMers398122864
23andMe allrs398122864
SNP Nexus

SNPshotrs398122864
SNPdbers398122864
MSV3drs398122864
GWAS Ctlgrs398122864
Max Magnitude0
ClinVar
Risk rs398122864(C;C)
Alt rs398122864(C;C)
Reference rs398122864(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.207643448G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000029133.23,