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rs137853038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853038(C;T)
Make rs137853038(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position41137768
GeneEP300
is asnp
is mentioned by
dbSNPrs137853038
ebirs137853038
HLIrs137853038
Exacrs137853038
Varsomers137853038
Maprs137853038
PheGenIrs137853038
hapmaprs137853038
1000 genomesrs137853038
hgdprs137853038
ensemblrs137853038
gopubmedrs137853038
geneviewrs137853038
scholarrs137853038
googlers137853038
pharmgkbrs137853038
gwascentralrs137853038
openSNPrs137853038
23andMers137853038
23andMe allrs137853038
SNP Nexus

SNPshotrs137853038
SNPdbers137853038
MSV3drs137853038
GWAS Ctlgrs137853038
Max Magnitude0
OMIM602700
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853038(T;T)
Alt rs137853038(T;T)
Reference rs137853038(C;C)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene EP300
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000022.10:g.41533772C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007283.6,