Have questions? Visit https://www.reddit.com/r/SNPedia

rs72553882

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72553882(C;G)
Make rs72553882(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position16940465
GeneTNFRSF13B
is asnp
is mentioned by
dbSNPrs72553882
ebirs72553882
HLIrs72553882
Exacrs72553882
Varsomers72553882
Maprs72553882
PheGenIrs72553882
hapmaprs72553882
1000 genomesrs72553882
hgdprs72553882
ensemblrs72553882
gopubmedrs72553882
geneviewrs72553882
scholarrs72553882
googlers72553882
pharmgkbrs72553882
gwascentralrs72553882
openSNPrs72553882
23andMers72553882
23andMe allrs72553882
SNP Nexus

SNPshotrs72553882
SNPdbers72553882
MSV3drs72553882
GWAS Ctlgrs72553882
Max Magnitude0
ClinVar
Risk rs72553882(A,G;A,G)
Alt rs72553882(A,G;A,G)
Reference rs72553882(C;C)
Significance Pathogenic
Disease Common variable immunodeficiency 2 Immunoglobulin A deficiency 2
Variation info
Gene TNFRSF13B
CLNDBN Common variable immunodeficiency 2 Immunoglobulin A deficiency 2
Reversed 1
HGVS NC_000017.10:g.16843779G>C
CLNSRC
CLNACC RCV000185537.2, RCV000185538.2,