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rs397515807

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515807(G;G)
Make rs397515807(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48470729
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515807
ebirs397515807
HLIrs397515807
Exacrs397515807
Varsomers397515807
Maprs397515807
PheGenIrs397515807
hapmaprs397515807
1000 genomesrs397515807
hgdprs397515807
ensemblrs397515807
gopubmedrs397515807
geneviewrs397515807
scholarrs397515807
googlers397515807
pharmgkbrs397515807
gwascentralrs397515807
openSNPrs397515807
23andMers397515807
23andMe allrs397515807
SNP Nexus

SNPshotrs397515807
SNPdbers397515807
MSV3drs397515807
GWAS Ctlgrs397515807
Max Magnitude0
ClinVar
Risk rs397515807(G;G)
Alt rs397515807(G;G)
Reference rs397515807(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48762926A>C
CLNSRC ClinVar
CLNACC RCV000035198.2,