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rs267606871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606871(A;C)
Make rs267606871(C;C)
ReferenceGRCh38 38.1/142
Chromosome14
Position105854468
GeneIGH@
is asnp
is mentioned by
dbSNPrs267606871
ebirs267606871
HLIrs267606871
Exacrs267606871
Varsomers267606871
Maprs267606871
PheGenIrs267606871
hapmaprs267606871
1000 genomesrs267606871
hgdprs267606871
ensemblrs267606871
gopubmedrs267606871
geneviewrs267606871
scholarrs267606871
googlers267606871
pharmgkbrs267606871
gwascentralrs267606871
openSNPrs267606871
23andMers267606871
23andMe allrs267606871
SNP Nexus

SNPshotrs267606871
SNPdbers267606871
MSV3drs267606871
GWAS Ctlgrs267606871
Max Magnitude0
ClinVar
Risk rs267606871(C;C)
Alt rs267606871(C;C)
Reference rs267606871(A;A)
Significance Untested
Disease Agammaglobulinemia
Variation info
Gene
CLNDBN Agammaglobulinemia, non-Bruton type
Reversed 0
HGVS NC_000014.8:g.106320573A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000144362.1,