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rs193922464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922464(C;T)
Make rs193922464(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position36573626
GeneRAG1
is asnp
is mentioned by
dbSNPrs193922464
ebirs193922464
HLIrs193922464
Exacrs193922464
Varsomers193922464
Maprs193922464
PheGenIrs193922464
hapmaprs193922464
1000 genomesrs193922464
hgdprs193922464
ensemblrs193922464
gopubmedrs193922464
geneviewrs193922464
scholarrs193922464
googlers193922464
pharmgkbrs193922464
gwascentralrs193922464
openSNPrs193922464
23andMers193922464
23andMe allrs193922464
SNP Nexus

SNPshotrs193922464
SNPdbers193922464
MSV3drs193922464
GWAS Ctlgrs193922464
Max Magnitude0
ClinVar
Risk rs193922464(G,T;G,T)
Alt rs193922464(G,T;G,T)
Reference rs193922464(C;C)
Significance Probable-Pathogenic
Disease Severe combined immunodeficiency disease
Variation info
Gene RAG1
CLNDBN Severe combined immunodeficiency disease
Reversed 0
HGVS NC_000011.9:g.36595176C>T
CLNSRC ClinVar
CLNACC RCV000030393.1,