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rs34562254

From SNPedia

Orientationminus
Stabilizedminus
Make rs34562254(C;C)
Make rs34562254(C;T)
Make rs34562254(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position16939677
GeneTNFRSF13B
is asnp
is mentioned by
dbSNPrs34562254
ClinGenrs34562254
ebirs34562254
HLIrs34562254
Exacrs34562254
Varsomers34562254
Maprs34562254
PheGenIrs34562254
hapmaprs34562254
1000 genomesrs34562254
hgdprs34562254
ensemblrs34562254
gopubmedrs34562254
geneviewrs34562254
scholarrs34562254
googlers34562254
pharmgkbrs34562254
gwascentralrs34562254
openSNPrs34562254
23andMers34562254
23andMe allrs34562254
SNP Nexus

SNPshotrs34562254
SNPdbers34562254
MSV3drs34562254
GWAS Ctlgrs34562254
Max Magnitude
ClinVar
Risk rs34562254(T;T)
Alt rs34562254(T;T)
Reference rs34562254(C;C)
Significance Non-pathogenic
Disease Common Variable Immune Deficiency not specified
Variation info
Gene TNFRSF13B
CLNDBN Common Variable Immune Deficiency, Dominant not specified
Reversed 1
HGVS NC_000017.10:g.16842991G>A
CLNSRC
CLNACC RCV000312789.1, RCV000455556.1,