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rs199469662

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199469662(C;T)
Make rs199469662(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position150828304
GeneLRBA
is asnp
is mentioned by
dbSNPrs199469662
ebirs199469662
HLIrs199469662
Exacrs199469662
Varsomers199469662
Maprs199469662
PheGenIrs199469662
hapmaprs199469662
1000 genomesrs199469662
hgdprs199469662
ensemblrs199469662
gopubmedrs199469662
geneviewrs199469662
scholarrs199469662
googlers199469662
pharmgkbrs199469662
gwascentralrs199469662
openSNPrs199469662
23andMers199469662
23andMe allrs199469662
SNP Nexus

SNPshotrs199469662
SNPdbers199469662
MSV3drs199469662
GWAS Ctlgrs199469662
Max Magnitude0
ClinVar
Risk rs199469662(T;T)
Alt rs199469662(T;T)
Reference rs199469662(C;C)
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.151749456G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000029135.5,