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

rs35062843

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs35062843(G;G)
Make rs35062843(G;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position16948892
GeneTNFRSF13B
is asnp
is mentioned by
dbSNPrs35062843
ClinGenrs35062843
ebirs35062843
HLIrs35062843
Exacrs35062843
Varsomers35062843
Maprs35062843
PheGenIrs35062843
hapmaprs35062843
1000 genomesrs35062843
hgdprs35062843
ensemblrs35062843
gopubmedrs35062843
geneviewrs35062843
scholarrs35062843
googlers35062843
pharmgkbrs35062843
gwascentralrs35062843
openSNPrs35062843
23andMers35062843
23andMe allrs35062843
SNP Nexus

SNPshotrs35062843
SNPdbers35062843
MSV3drs35062843
GWAS Ctlgrs35062843
GMAF0.02801
Max Magnitude0

[PMID 19775471OA-icon.png] Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8


ClinVar
Risk rs35062843(G;G)
Alt rs35062843(G;G)
Reference Rs35062843(T;T)
Significance Probable-non-pathogenic
Disease not specified Common Variable Immune Deficiency
Variation info
Gene TNFRSF13B
CLNDBN not specified Common Variable Immune Deficiency, Dominant
Reversed 1
HGVS NC_000017.10:g.16852206A>C
CLNSRC
CLNACC RCV000252622.1, RCV000359099.1,