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rs397515753

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515753(C;T)
Make rs397515753(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48520755
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515753
ebirs397515753
HLIrs397515753
Exacrs397515753
Varsomers397515753
Maprs397515753
PheGenIrs397515753
hapmaprs397515753
1000 genomesrs397515753
hgdprs397515753
ensemblrs397515753
gopubmedrs397515753
geneviewrs397515753
scholarrs397515753
googlers397515753
pharmgkbrs397515753
gwascentralrs397515753
openSNPrs397515753
23andMers397515753
23andMe allrs397515753
SNP Nexus

SNPshotrs397515753
SNPdbers397515753
MSV3drs397515753
GWAS Ctlgrs397515753
Max Magnitude0
ClinVar
Risk rs397515753(T;T)
Alt rs397515753(T;T)
Reference rs397515753(C;C)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48812952G>A
CLNSRC ClinVar
CLNACC RCV000035113.2,