Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507492

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507492(C;C)
Make rs397507492(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position119278271
GeneCBL
is asnp
is mentioned by
dbSNPrs397507492
ebirs397507492
HLIrs397507492
Exacrs397507492
Varsomers397507492
Maprs397507492
PheGenIrs397507492
hapmaprs397507492
1000 genomesrs397507492
hgdprs397507492
ensemblrs397507492
gopubmedrs397507492
geneviewrs397507492
scholarrs397507492
googlers397507492
pharmgkbrs397507492
gwascentralrs397507492
openSNPrs397507492
23andMers397507492
23andMe allrs397507492
SNP Nexus

SNPshotrs397507492
SNPdbers397507492
MSV3drs397507492
GWAS Ctlgrs397507492
Max Magnitude0
ClinVar
Risk rs397507492(C;C)
Alt rs397507492(C;C)
Reference rs397507492(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CBL
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.119148981T>C
CLNSRC ClinVar
CLNACC RCV000033354.4,