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rs727503779

From SNPedia

Orientationminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs727503779(-;-)
Make rs727503779(-;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position150471666
GeneLRBA
is asnp
is mentioned by
dbSNPrs727503779
ebirs727503779
HLIrs727503779
Exacrs727503779
Varsomers727503779
Maprs727503779
PheGenIrs727503779
hapmaprs727503779
1000 genomesrs727503779
hgdprs727503779
ensemblrs727503779
gopubmedrs727503779
geneviewrs727503779
scholarrs727503779
googlers727503779
pharmgkbrs727503779
gwascentralrs727503779
openSNPrs727503779
23andMers727503779
23andMe allrs727503779
SNP Nexus

SNPshotrs727503779
SNPdbers727503779
MSV3drs727503779
GWAS Ctlgrs727503779
Max Magnitude0
ClinVar
Risk rs727503779(;)
Alt rs727503779(;)
Reference rs727503779(GA;GA)
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.151392818_151392819delTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000150103.4,