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rs377767352

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377767352(-;-)
Make rs377767352(-;C)
ReferenceGRCh38 38.1/141
Chromosome18
Position51065580
GeneSMAD4
is asnp
is mentioned by
dbSNPrs377767352
ebirs377767352
HLIrs377767352
Exacrs377767352
Varsomers377767352
Maprs377767352
PheGenIrs377767352
hapmaprs377767352
1000 genomesrs377767352
hgdprs377767352
ensemblrs377767352
gopubmedrs377767352
geneviewrs377767352
scholarrs377767352
googlers377767352
pharmgkbrs377767352
gwascentralrs377767352
openSNPrs377767352
23andMers377767352
23andMe allrs377767352
SNP Nexus

SNPshotrs377767352
SNPdbers377767352
MSV3drs377767352
GWAS Ctlgrs377767352
Max Magnitude0
ClinVar
Risk rs377767352(;)
Alt rs377767352(;)
Reference rs377767352(C;C)
Significance Pathogenic
Disease Juvenile polyposis syndrome
Variation info
Gene SMAD4
CLNDBN Juvenile polyposis syndrome
Reversed 0
HGVS NC_000018.9:g.48591950delC
CLNSRC ClinVar
CLNACC RCV000021718.1,


[PMID 16436638OA-icon.png] Mutation screening in juvenile polyposis syndrome.