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rs121918684

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918684(C;C)
Make rs121918684(C;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position127738379
GeneMYC
is asnp
is mentioned by
dbSNPrs121918684
ebirs121918684
HLIrs121918684
Exacrs121918684
Varsomers121918684
Maprs121918684
PheGenIrs121918684
hapmaprs121918684
1000 genomesrs121918684
hgdprs121918684
ensemblrs121918684
gopubmedrs121918684
geneviewrs121918684
scholarrs121918684
googlers121918684
pharmgkbrs121918684
gwascentralrs121918684
openSNPrs121918684
23andMers121918684
23andMe allrs121918684
SNP Nexus

SNPshotrs121918684
SNPdbers121918684
MSV3drs121918684
GWAS Ctlgrs121918684
Max Magnitude0
OMIM190080
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918684(C;C)
Alt rs121918684(C;C)
Reference rs121918684(G;G)
Significance Pathogenic
Disease Burkitt lymphoma
Variation info
Gene MYC
CLNDBN Burkitt lymphoma
Reversed 0
HGVS NC_000008.10:g.128750625G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013404.18,