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

rs267606711

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606711(C;T)
Make rs267606711(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position63930266
GeneCD79B
is asnp
is mentioned by
dbSNPrs267606711
ebirs267606711
HLIrs267606711
Exacrs267606711
Varsomers267606711
Maprs267606711
PheGenIrs267606711
hapmaprs267606711
1000 genomesrs267606711
hgdprs267606711
ensemblrs267606711
gopubmedrs267606711
geneviewrs267606711
scholarrs267606711
googlers267606711
pharmgkbrs267606711
gwascentralrs267606711
openSNPrs267606711
23andMers267606711
23andMe allrs267606711
SNP Nexus

SNPshotrs267606711
SNPdbers267606711
MSV3drs267606711
GWAS Ctlgrs267606711
Max Magnitude0
ClinVar
Risk rs267606711(T;T)
Alt rs267606711(T;T)
Reference rs267606711(C;C)
Significance Pathogenic
Disease Agammaglobulinemia 6
Variation info
Gene CD79B
CLNDBN Agammaglobulinemia 6, autosomal recessive
Reversed 1
HGVS NC_000017.10:g.62007626G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015926.21,