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rs397515798

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515798(C;C)
Make rs397515798(C;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48474599
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515798
ebirs397515798
HLIrs397515798
Exacrs397515798
Varsomers397515798
Maprs397515798
PheGenIrs397515798
hapmaprs397515798
1000 genomesrs397515798
hgdprs397515798
ensemblrs397515798
gopubmedrs397515798
geneviewrs397515798
scholarrs397515798
googlers397515798
pharmgkbrs397515798
gwascentralrs397515798
openSNPrs397515798
23andMers397515798
23andMe allrs397515798
SNP Nexus

SNPshotrs397515798
SNPdbers397515798
MSV3drs397515798
GWAS Ctlgrs397515798
Max Magnitude0
ClinVar
Risk rs397515798(C;C)
Alt rs397515798(C;C)
Reference rs397515798(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48766796C>G
CLNSRC ClinVar
CLNACC RCV000035185.2,