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rs397515821

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515821(C;T)
Make rs397515821(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48452670
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515821
ebirs397515821
HLIrs397515821
Exacrs397515821
Varsomers397515821
Maprs397515821
PheGenIrs397515821
hapmaprs397515821
1000 genomesrs397515821
hgdprs397515821
ensemblrs397515821
gopubmedrs397515821
geneviewrs397515821
scholarrs397515821
googlers397515821
pharmgkbrs397515821
gwascentralrs397515821
openSNPrs397515821
23andMers397515821
23andMe allrs397515821
SNP Nexus

SNPshotrs397515821
SNPdbers397515821
MSV3drs397515821
GWAS Ctlgrs397515821
Max Magnitude0
ClinVar
Risk rs397515821(T;T)
Alt rs397515821(T;T)
Reference rs397515821(C;C)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48744867G>A
CLNSRC ClinVar
CLNACC RCV000035225.2,