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rs34557412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs34557412(C;C)
Make rs34557412(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position16948873
GeneTNFRSF13B
is asnp
is mentioned by
dbSNPrs34557412
ebirs34557412
HLIrs34557412
Exacrs34557412
Varsomers34557412
Maprs34557412
PheGenIrs34557412
hapmaprs34557412
1000 genomesrs34557412
hgdprs34557412
ensemblrs34557412
gopubmedrs34557412
geneviewrs34557412
scholarrs34557412
googlers34557412
pharmgkbrs34557412
gwascentralrs34557412
openSNPrs34557412
23andMers34557412
23andMe allrs34557412
SNP Nexus

SNPshotrs34557412
SNPdbers34557412
MSV3drs34557412
GWAS Ctlgrs34557412
GMAF0.003214
Max Magnitude0
OMIM604907
Desc
Variant0001
Relatedalso


ClinVar
Risk rs34557412(C;C)
Alt rs34557412(C;C)
Reference rs34557412(T;T)
Significance Other
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.16852187A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005623.2, RCV000005624.2,