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rs28937578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs28937578(A;A)
Make rs28937578(A;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position41178373
GeneEP300
is asnp
is mentioned by
dbSNPrs28937578
ebirs28937578
HLIrs28937578
Exacrs28937578
Varsomers28937578
Maprs28937578
PheGenIrs28937578
hapmaprs28937578
1000 genomesrs28937578
hgdprs28937578
ensemblrs28937578
gopubmedrs28937578
geneviewrs28937578
scholarrs28937578
googlers28937578
pharmgkbrs28937578
gwascentralrs28937578
openSNPrs28937578
23andMers28937578
23andMe allrs28937578
SNP Nexus

SNPshotrs28937578
SNPdbers28937578
MSV3drs28937578
GWAS Ctlgrs28937578
Max Magnitude0
OMIM602700
DescCOLORECTAL CANCER
Variant0002
Relatedalso


ClinVar
Risk rs28937578(A,T;A,T)
Alt rs28937578(A,T;A,T)
Reference rs28937578(C;C)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene EP300
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000022.10:g.41574377C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007284.6,