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rs199676861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199676861(A;T)
Make rs199676861(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position118349868
GeneCD3G
is asnp
is mentioned by
dbSNPrs199676861
ebirs199676861
HLIrs199676861
Exacrs199676861
Varsomers199676861
Maprs199676861
PheGenIrs199676861
hapmaprs199676861
1000 genomesrs199676861
hgdprs199676861
ensemblrs199676861
gopubmedrs199676861
geneviewrs199676861
scholarrs199676861
googlers199676861
pharmgkbrs199676861
gwascentralrs199676861
openSNPrs199676861
23andMers199676861
23andMe allrs199676861
SNP Nexus

SNPshotrs199676861
SNPdbers199676861
MSV3drs199676861
GWAS Ctlgrs199676861
Max Magnitude0
ClinVar
Risk rs199676861(T;T)
Alt rs199676861(T;T)
Reference rs199676861(A;A)
Significance Pathogenic
Disease Immunodeficiency 17
Variation info
Gene CD3G
CLNDBN Immunodeficiency 17
Reversed 0
HGVS NC_000011.9:g.118220583A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087023.4,