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rs121918685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918685(C;G)
Make rs121918685(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position127738437
GeneMYC
is asnp
is mentioned by
dbSNPrs121918685
ebirs121918685
HLIrs121918685
Exacrs121918685
Varsomers121918685
Maprs121918685
PheGenIrs121918685
hapmaprs121918685
1000 genomesrs121918685
hgdprs121918685
ensemblrs121918685
gopubmedrs121918685
geneviewrs121918685
scholarrs121918685
googlers121918685
pharmgkbrs121918685
gwascentralrs121918685
openSNPrs121918685
23andMers121918685
23andMe allrs121918685
SNP Nexus

SNPshotrs121918685
SNPdbers121918685
MSV3drs121918685
GWAS Ctlgrs121918685
Max Magnitude0
OMIM190080
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121918685(G;G)
Alt rs121918685(G;G)
Reference rs121918685(C;C)
Significance Pathogenic
Disease Burkitt lymphoma
Variation info
Gene MYC
CLNDBN Burkitt lymphoma
Reversed 0
HGVS NC_000008.10:g.128750683C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013405.20,