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rs121912967

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912967(C;C)
Make rs121912967(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position52906134
GeneDCC
is asnp
is mentioned by
dbSNPrs121912967
ebirs121912967
HLIrs121912967
Exacrs121912967
Varsomers121912967
Maprs121912967
PheGenIrs121912967
hapmaprs121912967
1000 genomesrs121912967
hgdprs121912967
ensemblrs121912967
gopubmedrs121912967
geneviewrs121912967
scholarrs121912967
googlers121912967
pharmgkbrs121912967
gwascentralrs121912967
openSNPrs121912967
23andMers121912967
23andMe allrs121912967
SNP Nexus

SNPshotrs121912967
SNPdbers121912967
MSV3drs121912967
GWAS Ctlgrs121912967
Max Magnitude0
OMIM120470
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912967(C;C)
Alt rs121912967(C;C)
Reference rs121912967(T;T)
Significance Pathogenic
Disease Esophageal carcinoma
Variation info
Gene DCC
CLNDBN Esophageal carcinoma, somatic
Reversed 0
HGVS NC_000018.9:g.50432504T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000018604.4,