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rs397507489

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507489(G;G)
Make rs397507489(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position119232558
GeneCBL
is asnp
is mentioned by
dbSNPrs397507489
ebirs397507489
HLIrs397507489
Exacrs397507489
Varsomers397507489
Maprs397507489
PheGenIrs397507489
hapmaprs397507489
1000 genomesrs397507489
hgdprs397507489
ensemblrs397507489
gopubmedrs397507489
geneviewrs397507489
scholarrs397507489
googlers397507489
pharmgkbrs397507489
gwascentralrs397507489
openSNPrs397507489
23andMers397507489
23andMe allrs397507489
SNP Nexus

SNPshotrs397507489
SNPdbers397507489
MSV3drs397507489
GWAS Ctlgrs397507489
Max Magnitude0
ClinVar
Risk rs397507489(G;G)
Alt rs397507489(G;G)
Reference rs397507489(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CBL
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.119103268T>G
CLNSRC ClinVar
CLNACC RCV000033348.4,