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rs104894650

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894650(A;A)
Make rs104894650(A;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position16948752
GeneTNFRSF13B
is asnp
is mentioned by
dbSNPrs104894650
ebirs104894650
HLIrs104894650
Exacrs104894650
Varsomers104894650
Maprs104894650
PheGenIrs104894650
hapmaprs104894650
1000 genomesrs104894650
hgdprs104894650
ensemblrs104894650
gopubmedrs104894650
geneviewrs104894650
scholarrs104894650
googlers104894650
pharmgkbrs104894650
gwascentralrs104894650
openSNPrs104894650
23andMers104894650
23andMe allrs104894650
SNP Nexus

SNPshotrs104894650
SNPdbers104894650
MSV3drs104894650
GWAS Ctlgrs104894650
Max Magnitude0
OMIM604907
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894650(A,G,T;A,G,T)
Alt rs104894650(A,G,T;A,G,T)
Reference rs104894650(C;C)
Significance Pathogenic
Disease Common variable immunodeficiency 2
Variation info
Gene TNFRSF13B
CLNDBN Common variable immunodeficiency 2
Reversed 1
HGVS NC_000017.10:g.16852066G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005631.2,