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rs36001797

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs36001797(A;A)
Make rs36001797(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position36593886
GeneC11orf74, RAG2
is asnp
is mentioned by
dbSNPrs36001797
ebirs36001797
HLIrs36001797
Exacrs36001797
Varsomers36001797
Maprs36001797
PheGenIrs36001797
hapmaprs36001797
1000 genomesrs36001797
hgdprs36001797
ensemblrs36001797
gopubmedrs36001797
geneviewrs36001797
scholarrs36001797
googlers36001797
pharmgkbrs36001797
gwascentralrs36001797
openSNPrs36001797
23andMers36001797
23andMe allrs36001797
SNP Nexus

SNPshotrs36001797
SNPdbers36001797
MSV3drs36001797
GWAS Ctlgrs36001797
Max Magnitude0
OMIM179616
Desc
Variant0005
Relatedalso


ClinVar
Risk rs36001797(A;A)
Alt rs36001797(A;A)
Reference rs36001797(G;G)
Significance Pathogenic
Disease Histiocytic medullary reticulosis
Variation info
Gene RAG2 C11orf74
CLNDBN Histiocytic medullary reticulosis
Reversed 1
HGVS NC_000011.9:g.36615436C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014014.24,