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rs387906665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906665(C;C)
Make rs387906665(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position119278256
GeneCBL
is asnp
is mentioned by
dbSNPrs387906665
ebirs387906665
HLIrs387906665
Exacrs387906665
Varsomers387906665
Maprs387906665
PheGenIrs387906665
hapmaprs387906665
1000 genomesrs387906665
hgdprs387906665
ensemblrs387906665
gopubmedrs387906665
geneviewrs387906665
scholarrs387906665
googlers387906665
pharmgkbrs387906665
gwascentralrs387906665
openSNPrs387906665
23andMers387906665
23andMe allrs387906665
SNP Nexus

SNPshotrs387906665
SNPdbers387906665
MSV3drs387906665
GWAS Ctlgrs387906665
Max Magnitude0
ClinVar
Risk rs387906665(C;C)
Alt rs387906665(C;C)
Reference rs387906665(T;T)
Significance Pathogenic
Disease Noonan syndrome-like disorder with juvenile myelomonocytic leukemia not provided
Variation info
Gene CBL
CLNDBN Noonan syndrome-like disorder with juvenile myelomonocytic leukemia not provided
Reversed 0
HGVS NC_000011.9:g.119148966T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022699.21, RCV000157860.1,