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rs121918568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918568(C;T)
Make rs121918568(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position36574244
GeneRAG1
is asnp
is mentioned by
dbSNPrs121918568
ebirs121918568
HLIrs121918568
Exacrs121918568
Varsomers121918568
Maprs121918568
PheGenIrs121918568
hapmaprs121918568
1000 genomesrs121918568
hgdprs121918568
ensemblrs121918568
gopubmedrs121918568
geneviewrs121918568
scholarrs121918568
googlers121918568
pharmgkbrs121918568
gwascentralrs121918568
openSNPrs121918568
23andMers121918568
23andMe allrs121918568
SNP Nexus

SNPshotrs121918568
SNPdbers121918568
MSV3drs121918568
GWAS Ctlgrs121918568
Max Magnitude0
OMIM179615
Desc
Variant0018
Relatedalso
ClinVar
Risk rs121918568(T;T)
Alt rs121918568(T;T)
Reference rs121918568(C;C)
Significance Pathogenic
Disease Combined cellular and humoral immune defects with granulomas
Variation info
Gene RAG1
CLNDBN Combined cellular and humoral immune defects with granulomas
Reversed 0
HGVS NC_000011.9:g.36595794C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014042.24,