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rs397515766

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515766(C;C)
Make rs397515766(C;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48496178
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515766
ebirs397515766
HLIrs397515766
Exacrs397515766
Varsomers397515766
Maprs397515766
PheGenIrs397515766
hapmaprs397515766
1000 genomesrs397515766
hgdprs397515766
ensemblrs397515766
gopubmedrs397515766
geneviewrs397515766
scholarrs397515766
googlers397515766
pharmgkbrs397515766
gwascentralrs397515766
openSNPrs397515766
23andMers397515766
23andMe allrs397515766
SNP Nexus

SNPshotrs397515766
SNPdbers397515766
MSV3drs397515766
GWAS Ctlgrs397515766
Max Magnitude0
ClinVar
Risk rs397515766(C;C)
Alt rs397515766(C;C)
Reference rs397515766(T;T)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48788375A>G
CLNSRC ClinVar
CLNACC RCV000035135.2,