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rs772340017

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs772340017(A;G)
Make rs772340017(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position36574742
GeneRAG1
is asnp
is mentioned by
dbSNPrs772340017
ebirs772340017
HLIrs772340017
Exacrs772340017
Varsomers772340017
Maprs772340017
PheGenIrs772340017
hapmaprs772340017
1000 genomesrs772340017
hgdprs772340017
ensemblrs772340017
gopubmedrs772340017
geneviewrs772340017
scholarrs772340017
googlers772340017
pharmgkbrs772340017
gwascentralrs772340017
openSNPrs772340017
23andMers772340017
23andMe allrs772340017
SNP Nexus

SNPshotrs772340017
SNPdbers772340017
MSV3drs772340017
GWAS Ctlgrs772340017
Max Magnitude0
ClinVar
Risk rs772340017(G;G)
Alt rs772340017(G;G)
Reference rs772340017(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAG1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.36596292A>G
CLNSRC
CLNACC RCV000171192.1,