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rs483352928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs483352928(C;C)
Make rs483352928(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position118313876
GeneCD3E
is asnp
is mentioned by
dbSNPrs483352928
ebirs483352928
HLIrs483352928
Exacrs483352928
Varsomers483352928
Maprs483352928
PheGenIrs483352928
hapmaprs483352928
1000 genomesrs483352928
hgdprs483352928
ensemblrs483352928
gopubmedrs483352928
geneviewrs483352928
scholarrs483352928
googlers483352928
pharmgkbrs483352928
gwascentralrs483352928
openSNPrs483352928
23andMers483352928
23andMe allrs483352928
SNP Nexus

SNPshotrs483352928
SNPdbers483352928
MSV3drs483352928
GWAS Ctlgrs483352928
Max Magnitude0
ClinVar
Risk rs483352928(C;C)
Alt rs483352928(C;C)
Reference rs483352928(T;T)
Significance Pathogenic
Disease Immunodeficiency 18
Variation info
Gene CD3E
CLNDBN Immunodeficiency 18
Reversed 0
HGVS NC_000011.9:g.118184591T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000087024.4,