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rs377767381

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377767381(C;G)
Make rs377767381(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position51078405
GeneSMAD4
is asnp
is mentioned by
dbSNPrs377767381
ebirs377767381
HLIrs377767381
Exacrs377767381
Varsomers377767381
Maprs377767381
PheGenIrs377767381
hapmaprs377767381
1000 genomesrs377767381
hgdprs377767381
ensemblrs377767381
gopubmedrs377767381
geneviewrs377767381
scholarrs377767381
googlers377767381
pharmgkbrs377767381
gwascentralrs377767381
openSNPrs377767381
23andMers377767381
23andMe allrs377767381
SNP Nexus

SNPshotrs377767381
SNPdbers377767381
MSV3drs377767381
GWAS Ctlgrs377767381
Max Magnitude0
ClinVar
Risk rs377767381(G;G)
Alt rs377767381(G;G)
Reference rs377767381(C;C)
Significance Pathogenic
Disease Juvenile polyposis syndrome
Variation info
Gene SMAD4
CLNDBN Juvenile polyposis syndrome
Reversed 0
HGVS NC_000018.9:g.48604775C>G
CLNSRC ARUP SMAD4
CLNACC RCV000021754.1,


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