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rs377767326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377767326(C;T)
Make rs377767326(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position51048839
GeneSMAD4
is asnp
is mentioned by
dbSNPrs377767326
ebirs377767326
HLIrs377767326
Exacrs377767326
Varsomers377767326
Maprs377767326
PheGenIrs377767326
hapmaprs377767326
1000 genomesrs377767326
hgdprs377767326
ensemblrs377767326
gopubmedrs377767326
geneviewrs377767326
scholarrs377767326
googlers377767326
pharmgkbrs377767326
gwascentralrs377767326
openSNPrs377767326
23andMers377767326
23andMe allrs377767326
SNP Nexus

SNPshotrs377767326
SNPdbers377767326
MSV3drs377767326
GWAS Ctlgrs377767326
Max Magnitude0
ClinVar
Risk rs377767326(T;T)
Alt rs377767326(T;T)
Reference rs377767326(C;C)
Significance Pathogenic
Disease Juvenile polyposis syndrome
Variation info
Gene SMAD4
CLNDBN Juvenile polyposis syndrome
Reversed 0
HGVS NC_000018.9:g.48575209C>T
CLNSRC ARUP SMAD4
CLNACC RCV000021682.1,


[PMID 15814640] SMAD4 as a prognostic marker in colorectal cancer.