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rs397507491

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507491(G;G)
Make rs397507491(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position119278269
GeneCBL
is asnp
is mentioned by
dbSNPrs397507491
ebirs397507491
HLIrs397507491
Exacrs397507491
Varsomers397507491
Maprs397507491
PheGenIrs397507491
hapmaprs397507491
1000 genomesrs397507491
hgdprs397507491
ensemblrs397507491
gopubmedrs397507491
geneviewrs397507491
scholarrs397507491
googlers397507491
pharmgkbrs397507491
gwascentralrs397507491
openSNPrs397507491
23andMers397507491
23andMe allrs397507491
SNP Nexus

SNPshotrs397507491
SNPdbers397507491
MSV3drs397507491
GWAS Ctlgrs397507491
Max Magnitude0
ClinVar
Risk rs397507491(G;G)
Alt rs397507491(G;G)
Reference rs397507491(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CBL
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.119148979T>G
CLNSRC ClinVar
CLNACC RCV000033353.3,