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rs121918659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918659(A;A)
Make rs121918659(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position118312690
GeneCD3E
is asnp
is mentioned by
dbSNPrs121918659
ebirs121918659
HLIrs121918659
Exacrs121918659
Varsomers121918659
Maprs121918659
PheGenIrs121918659
hapmaprs121918659
1000 genomesrs121918659
hgdprs121918659
ensemblrs121918659
gopubmedrs121918659
geneviewrs121918659
scholarrs121918659
googlers121918659
pharmgkbrs121918659
gwascentralrs121918659
openSNPrs121918659
23andMers121918659
23andMe allrs121918659
SNP Nexus

SNPshotrs121918659
SNPdbers121918659
MSV3drs121918659
GWAS Ctlgrs121918659
Max Magnitude0
OMIM186830
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918659(A;A)
Alt rs121918659(A;A)
Reference rs121918659(G;G)
Significance Pathogenic
Disease Immunodeficiency 18
Variation info
Gene CD3E
CLNDBN Immunodeficiency 18
Reversed 0
HGVS NC_000011.9:g.118183405G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087025.6,