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rs104894284

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894284(A;A)
Make rs104894284(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position36574986
GeneRAG1
is asnp
is mentioned by
dbSNPrs104894284
ebirs104894284
HLIrs104894284
Exacrs104894284
Varsomers104894284
Maprs104894284
PheGenIrs104894284
hapmaprs104894284
1000 genomesrs104894284
hgdprs104894284
ensemblrs104894284
gopubmedrs104894284
geneviewrs104894284
scholarrs104894284
googlers104894284
pharmgkbrs104894284
gwascentralrs104894284
openSNPrs104894284
23andMers104894284
23andMe allrs104894284
SNP Nexus

SNPshotrs104894284
SNPdbers104894284
MSV3drs104894284
GWAS Ctlgrs104894284
Max Magnitude0
OMIM179615
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894284(A;A)
Alt rs104894284(A;A)
Reference rs104894284(G;G)
Significance Pathogenic
Disease Histiocytic medullary reticulosis
Variation info
Gene RAG1
CLNDBN Histiocytic medullary reticulosis
Reversed 0
HGVS NC_000011.9:g.36596536G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014025.18,