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rs397507493

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TAC;TAC) 0 common in clinvar
Make rs397507493(AAG;AAG)
Make rs397507493(AAG;TAC)
ReferenceGRCh38 38.1/141
Chromosome11
Position119278299
GeneCBL
is asnp
is mentioned by
dbSNPrs397507493
ebirs397507493
HLIrs397507493
Exacrs397507493
Varsomers397507493
Maprs397507493
PheGenIrs397507493
hapmaprs397507493
1000 genomesrs397507493
hgdprs397507493
ensemblrs397507493
gopubmedrs397507493
geneviewrs397507493
scholarrs397507493
googlers397507493
pharmgkbrs397507493
gwascentralrs397507493
openSNPrs397507493
23andMers397507493
23andMe allrs397507493
SNP Nexus

SNPshotrs397507493
SNPdbers397507493
MSV3drs397507493
GWAS Ctlgrs397507493
Max Magnitude0
ClinVar
Risk rs397507493(AAG;AAG)
Alt rs397507493(AAG;AAG)
Reference rs397507493(TAC;TAC)
Significance Pathogenic
Disease Rasopathy
Variation info
Gene CBL
CLNDBN Rasopathy
Reversed 0
HGVS NC_000011.9:g.119149009_119149011delTACinsAAG
CLNSRC ClinVar
CLNACC RCV000033355.2,