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rs104894199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894199(A;G)
Make rs104894199(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position118344424
GeneCD3D, CD3G
is asnp
is mentioned by
dbSNPrs104894199
ebirs104894199
HLIrs104894199
Exacrs104894199
Varsomers104894199
Maprs104894199
PheGenIrs104894199
hapmaprs104894199
1000 genomesrs104894199
hgdprs104894199
ensemblrs104894199
gopubmedrs104894199
geneviewrs104894199
scholarrs104894199
googlers104894199
pharmgkbrs104894199
gwascentralrs104894199
openSNPrs104894199
23andMers104894199
23andMe allrs104894199
SNP Nexus

SNPshotrs104894199
SNPdbers104894199
MSV3drs104894199
GWAS Ctlgrs104894199
Max Magnitude0
OMIM186740
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894199(G;G)
Alt rs104894199(G;G)
Reference rs104894199(A;A)
Significance Pathogenic
Disease Immunodeficiency 17
Variation info
Gene CD3D CD3G
CLNDBN Immunodeficiency 17
Reversed 0
HGVS NC_000011.9:g.118215139A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000087021.3,