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rs199469663

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199469663(G;G)
Make rs199469663(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position150302705
GeneLRBA
is asnp
is mentioned by
dbSNPrs199469663
ebirs199469663
HLIrs199469663
Exacrs199469663
Varsomers199469663
Maprs199469663
PheGenIrs199469663
hapmaprs199469663
1000 genomesrs199469663
hgdprs199469663
ensemblrs199469663
gopubmedrs199469663
geneviewrs199469663
scholarrs199469663
googlers199469663
pharmgkbrs199469663
gwascentralrs199469663
openSNPrs199469663
23andMers199469663
23andMe allrs199469663
SNP Nexus

SNPshotrs199469663
SNPdbers199469663
MSV3drs199469663
GWAS Ctlgrs199469663
Max Magnitude0
ClinVar
Risk rs199469663(G;G)
Alt rs199469663(G;G)
Reference rs199469663(T;T)
Significance Pathogenic
Disease Common variable immunodeficiency 8
Variation info
Gene LRBA
CLNDBN Common variable immunodeficiency 8, with autoimmunity
Reversed 1
HGVS NC_000004.11:g.151223857A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000029134.4,