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rs727504426

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504426(A;G)
Make rs727504426(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position119278508
GeneCBL
is asnp
is mentioned by
dbSNPrs727504426
ebirs727504426
HLIrs727504426
Exacrs727504426
Varsomers727504426
Maprs727504426
PheGenIrs727504426
hapmaprs727504426
1000 genomesrs727504426
hgdprs727504426
ensemblrs727504426
gopubmedrs727504426
geneviewrs727504426
scholarrs727504426
googlers727504426
pharmgkbrs727504426
gwascentralrs727504426
openSNPrs727504426
23andMers727504426
23andMe allrs727504426
SNP Nexus

SNPshotrs727504426
SNPdbers727504426
MSV3drs727504426
GWAS Ctlgrs727504426
Max Magnitude0
ClinVar
Risk rs727504426(G;G)
Alt rs727504426(G;G)
Reference rs727504426(A;A)
Significance Pathogenic
Disease Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Rasopathy Juvenile myelomonocytic leukemia
Variation info
Gene CBL
CLNDBN Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Rasopathy Juvenile myelomonocytic leukemia
Reversed 0
HGVS NC_000011.9:g.119149218A>G
CLNSRC
CLNACC RCV000154623.2, RCV000157861.1, RCV000220945.1,