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rs727503780

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503780(C;T)
Make rs727503780(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position150896429
GeneLRBA
is asnp
is mentioned by
dbSNPrs727503780
ebirs727503780
HLIrs727503780
Exacrs727503780
Varsomers727503780
Maprs727503780
PheGenIrs727503780
hapmaprs727503780
1000 genomesrs727503780
hgdprs727503780
ensemblrs727503780
gopubmedrs727503780
geneviewrs727503780
scholarrs727503780
googlers727503780
pharmgkbrs727503780
gwascentralrs727503780
openSNPrs727503780
23andMers727503780
23andMe allrs727503780
SNP Nexus

SNPshotrs727503780
SNPdbers727503780
MSV3drs727503780
GWAS Ctlgrs727503780
Max Magnitude0
ClinVar
Risk rs727503780(A,T;A,T)
Alt rs727503780(A,T;A,T)
Reference rs727503780(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.151817581G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000150104.4,