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rs121917896

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121917896(G;G)
Make rs121917896(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position36593315
GeneRAG2
is asnp
is mentioned by
dbSNPrs121917896
ebirs121917896
HLIrs121917896
Exacrs121917896
Varsomers121917896
Maprs121917896
PheGenIrs121917896
hapmaprs121917896
1000 genomesrs121917896
hgdprs121917896
ensemblrs121917896
gopubmedrs121917896
geneviewrs121917896
scholarrs121917896
googlers121917896
pharmgkbrs121917896
gwascentralrs121917896
openSNPrs121917896
23andMers121917896
23andMe allrs121917896
SNP Nexus

SNPshotrs121917896
SNPdbers121917896
MSV3drs121917896
GWAS Ctlgrs121917896
Max Magnitude0
ClinVar
Risk rs121917896(G;G)
Alt rs121917896(G;G)
Reference rs121917896(T;T)
Significance Pathogenic
Disease Histiocytic medullary reticulosis
Variation info
Gene RAG2 C11orf74
CLNDBN Histiocytic medullary reticulosis
Reversed 1
HGVS NC_000011.9:g.36614865A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014013.17,