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rs397515831

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515831(G;T)
Make rs397515831(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48437792
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515831
ebirs397515831
HLIrs397515831
Exacrs397515831
Varsomers397515831
Maprs397515831
PheGenIrs397515831
hapmaprs397515831
1000 genomesrs397515831
hgdprs397515831
ensemblrs397515831
gopubmedrs397515831
geneviewrs397515831
scholarrs397515831
googlers397515831
pharmgkbrs397515831
gwascentralrs397515831
openSNPrs397515831
23andMers397515831
23andMe allrs397515831
SNP Nexus

SNPshotrs397515831
SNPdbers397515831
MSV3drs397515831
GWAS Ctlgrs397515831
Max Magnitude0
ClinVar
Risk rs397515831(T;T)
Alt rs397515831(T;T)
Reference rs397515831(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48729989C>A
CLNSRC ClinVar
CLNACC RCV000035240.2,