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rs121917895

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917895(C;G)
Make rs121917895(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position36594046
GeneRAG2
is asnp
is mentioned by
dbSNPrs121917895
ebirs121917895
HLIrs121917895
Exacrs121917895
Varsomers121917895
Maprs121917895
PheGenIrs121917895
hapmaprs121917895
1000 genomesrs121917895
hgdprs121917895
ensemblrs121917895
gopubmedrs121917895
geneviewrs121917895
scholarrs121917895
googlers121917895
pharmgkbrs121917895
gwascentralrs121917895
openSNPrs121917895
23andMers121917895
23andMe allrs121917895
SNP Nexus

SNPshotrs121917895
SNPdbers121917895
MSV3drs121917895
GWAS Ctlgrs121917895
Max Magnitude0
ClinVar
Risk rs121917895(G,T;G,T)
Alt rs121917895(G,T;G,T)
Reference rs121917895(C;C)
Significance Pathogenic
Disease Histiocytic medullary reticulosis
Variation info
Gene RAG2 C11orf74
CLNDBN Histiocytic medullary reticulosis
Reversed 1
HGVS NC_000011.9:g.36615596G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014012.17,