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rs878853004

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853004(A;A)
Make rs878853004(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position36575309
GeneRAG1
is asnp
is mentioned by
dbSNPrs878853004
ebirs878853004
HLIrs878853004
Exacrs878853004
Varsomers878853004
Maprs878853004
PheGenIrs878853004
hapmaprs878853004
1000 genomesrs878853004
hgdprs878853004
ensemblrs878853004
gopubmedrs878853004
geneviewrs878853004
scholarrs878853004
googlers878853004
pharmgkbrs878853004
gwascentralrs878853004
openSNPrs878853004
23andMers878853004
23andMe allrs878853004
SNP Nexus

SNPshotrs878853004
SNPdbers878853004
MSV3drs878853004
GWAS Ctlgrs878853004
Max Magnitude0
ClinVar
Risk rs878853004(A;A)
Alt rs878853004(A;A)
Reference rs878853004(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAG1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.36596859G>A
CLNSRC
CLNACC RCV000223999.1,