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rs377767342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377767342(A;A)
Make rs377767342(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position51065455
GeneSMAD4
is asnp
is mentioned by
dbSNPrs377767342
ebirs377767342
HLIrs377767342
Exacrs377767342
Varsomers377767342
Maprs377767342
PheGenIrs377767342
hapmaprs377767342
1000 genomesrs377767342
hgdprs377767342
ensemblrs377767342
gopubmedrs377767342
geneviewrs377767342
scholarrs377767342
googlers377767342
pharmgkbrs377767342
gwascentralrs377767342
openSNPrs377767342
23andMers377767342
23andMe allrs377767342
SNP Nexus

SNPshotrs377767342
SNPdbers377767342
MSV3drs377767342
GWAS Ctlgrs377767342
Max Magnitude0
ClinVar
Risk rs377767342(A;A)
Alt rs377767342(A;A)
Reference rs377767342(G;G)
Significance Pathogenic
Disease JP and JP/HHT
Variation info
Gene SMAD4
CLNDBN JP and JP/HHT
Reversed 0
HGVS NC_000018.9:g.48591825G>A
CLNSRC ARUP SMAD4
CLNACC RCV000021703.1,


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