Have questions? Visit https://www.reddit.com/r/SNPedia

rs121918683

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918683(A;C)
Make rs121918683(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position127738519
GeneMYC
is asnp
is mentioned by
dbSNPrs121918683
ebirs121918683
HLIrs121918683
Exacrs121918683
Varsomers121918683
Maprs121918683
PheGenIrs121918683
hapmaprs121918683
1000 genomesrs121918683
hgdprs121918683
ensemblrs121918683
gopubmedrs121918683
geneviewrs121918683
scholarrs121918683
googlers121918683
pharmgkbrs121918683
gwascentralrs121918683
openSNPrs121918683
23andMers121918683
23andMe allrs121918683
SNP Nexus

SNPshotrs121918683
SNPdbers121918683
MSV3drs121918683
GWAS Ctlgrs121918683
Max Magnitude0
OMIM190080
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918683(C;C)
Alt rs121918683(C;C)
Reference rs121918683(A;A)
Significance Pathogenic
Disease Burkitt lymphoma
Variation info
Gene MYC
CLNDBN Burkitt lymphoma
Reversed 0
HGVS NC_000008.10:g.128750765A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013403.20,