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rs193922573

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922573(A;A)
Make rs193922573(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position36592860
GeneRAG2
is asnp
is mentioned by
dbSNPrs193922573
ebirs193922573
HLIrs193922573
Exacrs193922573
Varsomers193922573
Maprs193922573
PheGenIrs193922573
hapmaprs193922573
1000 genomesrs193922573
hgdprs193922573
ensemblrs193922573
gopubmedrs193922573
geneviewrs193922573
scholarrs193922573
googlers193922573
pharmgkbrs193922573
gwascentralrs193922573
openSNPrs193922573
23andMers193922573
23andMe allrs193922573
SNP Nexus

SNPshotrs193922573
SNPdbers193922573
MSV3drs193922573
GWAS Ctlgrs193922573
Max Magnitude0
ClinVar
Risk rs193922573(A;A)
Alt rs193922573(A;A)
Reference rs193922573(G;G)
Significance Probable-Pathogenic
Disease Severe combined immunodeficiency disease
Variation info
Gene RAG2 C11orf74
CLNDBN Severe combined immunodeficiency disease
Reversed 1
HGVS NC_000011.9:g.36614410C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030397.1,