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rs121912424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912424(A;A)
Make rs121912424(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position63930095
GeneCD79B
is asnp
is mentioned by
dbSNPrs121912424
ebirs121912424
HLIrs121912424
Exacrs121912424
Varsomers121912424
Maprs121912424
PheGenIrs121912424
hapmaprs121912424
1000 genomesrs121912424
hgdprs121912424
ensemblrs121912424
gopubmedrs121912424
geneviewrs121912424
scholarrs121912424
googlers121912424
pharmgkbrs121912424
gwascentralrs121912424
openSNPrs121912424
23andMers121912424
23andMe allrs121912424
SNP Nexus

SNPshotrs121912424
SNPdbers121912424
MSV3drs121912424
GWAS Ctlgrs121912424
Max Magnitude0
OMIM147245
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121912424(A;A)
Alt rs121912424(A;A)
Reference rs121912424(G;G)
Significance Pathogenic
Disease Agammaglobulinemia 6
Variation info
Gene CD79B
CLNDBN Agammaglobulinemia 6, autosomal recessive
Reversed 1
HGVS NC_000017.10:g.62007455C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015925.25,