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rs387906851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906851(C;T)
Make rs387906851(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position67181364
GeneSMAD3
is asnp
is mentioned by
dbSNPrs387906851
ebirs387906851
HLIrs387906851
Exacrs387906851
Varsomers387906851
Maprs387906851
PheGenIrs387906851
hapmaprs387906851
1000 genomesrs387906851
hgdprs387906851
ensemblrs387906851
gopubmedrs387906851
geneviewrs387906851
scholarrs387906851
googlers387906851
pharmgkbrs387906851
gwascentralrs387906851
openSNPrs387906851
23andMers387906851
23andMe allrs387906851
SNP Nexus

SNPshotrs387906851
SNPdbers387906851
MSV3drs387906851
GWAS Ctlgrs387906851
Max Magnitude0
ClinVar
Risk rs387906851(T;T)
Alt rs387906851(T;T)
Reference rs387906851(C;C)
Significance Pathogenic
Disease Loeys-Dietz syndrome 3
Variation info
Gene SMAD3
CLNDBN Loeys-Dietz syndrome 3
Reversed 0
HGVS NC_000015.9:g.67473702C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023243.3,