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rs387906555

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906555(A;A)
Make rs387906555(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position53526629
GeneDCC
is asnp
is mentioned by
dbSNPrs387906555
ebirs387906555
HLIrs387906555
Exacrs387906555
Varsomers387906555
Maprs387906555
PheGenIrs387906555
hapmaprs387906555
1000 genomesrs387906555
hgdprs387906555
ensemblrs387906555
gopubmedrs387906555
geneviewrs387906555
scholarrs387906555
googlers387906555
pharmgkbrs387906555
gwascentralrs387906555
openSNPrs387906555
23andMers387906555
23andMe allrs387906555
SNP Nexus

SNPshotrs387906555
SNPdbers387906555
MSV3drs387906555
GWAS Ctlgrs387906555
Max Magnitude0
ClinVar
Risk rs387906555(A,T;A,T)
Alt rs387906555(A,T;A,T)
Reference rs387906555(C;C)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene DCC
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000018.9:g.51052999C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018603.4,