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rs111033581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033581(A;A)
Make rs111033581(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position118339902
GeneCD3D
is asnp
is mentioned by
dbSNPrs111033581
ebirs111033581
HLIrs111033581
Exacrs111033581
Varsomers111033581
Maprs111033581
PheGenIrs111033581
hapmaprs111033581
1000 genomesrs111033581
hgdprs111033581
ensemblrs111033581
gopubmedrs111033581
geneviewrs111033581
scholarrs111033581
googlers111033581
pharmgkbrs111033581
gwascentralrs111033581
openSNPrs111033581
23andMers111033581
23andMe allrs111033581
SNP Nexus

SNPshotrs111033581
SNPdbers111033581
MSV3drs111033581
GWAS Ctlgrs111033581
Max Magnitude0
OMIM186790
Desc
Variant0002
Relatedalso
ClinVar
Risk rs111033581(A;A)
Alt rs111033581(A;A)
Reference rs111033581(C;C)
Significance Pathogenic
Disease Immunodeficiency 19
Variation info
Gene CD3D
CLNDBN Immunodeficiency 19
Reversed 1
HGVS NC_000011.9:g.118210617G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000083295.3,