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rs532338576

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs532338576(-;-)
Make rs532338576(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position23575031
GeneIGLL1
is asnp
is mentioned by
dbSNPrs532338576
ebirs532338576
HLIrs532338576
Exacrs532338576
Varsomers532338576
Maprs532338576
PheGenIrs532338576
hapmaprs532338576
1000 genomesrs532338576
hgdprs532338576
ensemblrs532338576
gopubmedrs532338576
geneviewrs532338576
scholarrs532338576
googlers532338576
pharmgkbrs532338576
gwascentralrs532338576
openSNPrs532338576
23andMers532338576
23andMe allrs532338576
SNP Nexus

SNPshotrs532338576
SNPdbers532338576
MSV3drs532338576
GWAS Ctlgrs532338576
Max Magnitude0
ClinVar
Risk rs532338576(;)
Alt rs532338576(;)
Reference rs532338576(C;C)
Significance Pathogenic
Disease Agammaglobulinemia 2
Variation info
Gene IGLL1
CLNDBN Agammaglobulinemia 2, autosomal recessive
Reversed 0
HGVS NC_000022.10:g.23917218delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000225003.1,