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rs387906666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906666(A;G)
Make rs387906666(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position119278182
GeneCBL
is asnp
is mentioned by
dbSNPrs387906666
ebirs387906666
HLIrs387906666
Exacrs387906666
Varsomers387906666
Maprs387906666
PheGenIrs387906666
hapmaprs387906666
1000 genomesrs387906666
hgdprs387906666
ensemblrs387906666
gopubmedrs387906666
geneviewrs387906666
scholarrs387906666
googlers387906666
pharmgkbrs387906666
gwascentralrs387906666
openSNPrs387906666
23andMers387906666
23andMe allrs387906666
SNP Nexus

SNPshotrs387906666
SNPdbers387906666
MSV3drs387906666
GWAS Ctlgrs387906666
Max Magnitude0
ClinVar
Risk rs387906666(G;G)
Alt rs387906666(G;G)
Reference rs387906666(A;A)
Significance Pathogenic
Disease Juvenile myelomonocytic leukemia Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Variation info
Gene CBL
CLNDBN Juvenile myelomonocytic leukemia Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Reversed 0
HGVS NC_000011.9:g.119148892A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022700.26, RCV000211127.1,