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rs28933407

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28933407(C;T)
Make rs28933407(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position127738431
GeneMYC
is asnp
is mentioned by
dbSNPrs28933407
ebirs28933407
HLIrs28933407
Exacrs28933407
Varsomers28933407
Maprs28933407
PheGenIrs28933407
hapmaprs28933407
1000 genomesrs28933407
hgdprs28933407
ensemblrs28933407
gopubmedrs28933407
geneviewrs28933407
scholarrs28933407
googlers28933407
pharmgkbrs28933407
gwascentralrs28933407
openSNPrs28933407
23andMers28933407
23andMe allrs28933407
SNP Nexus

SNPshotrs28933407
SNPdbers28933407
MSV3drs28933407
GWAS Ctlgrs28933407
Max Magnitude0
OMIM190080
DescBURKITT LYMPHOMA
Variant0001
Relatedalso


ClinVar
Risk rs28933407(T;T)
Alt rs28933407(T;T)
Reference rs28933407(C;C)
Significance Pathogenic
Disease Burkitt lymphoma
Variation info
Gene MYC
CLNDBN Burkitt lymphoma
Reversed 0
HGVS NC_000008.10:g.128750677C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013402.23,