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rs397515817

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515817(A;A)
Make rs397515817(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48464009
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515817
ebirs397515817
HLIrs397515817
Exacrs397515817
Varsomers397515817
Maprs397515817
PheGenIrs397515817
hapmaprs397515817
1000 genomesrs397515817
hgdprs397515817
ensemblrs397515817
gopubmedrs397515817
geneviewrs397515817
scholarrs397515817
googlers397515817
pharmgkbrs397515817
gwascentralrs397515817
openSNPrs397515817
23andMers397515817
23andMe allrs397515817
SNP Nexus

SNPshotrs397515817
SNPdbers397515817
MSV3drs397515817
GWAS Ctlgrs397515817
Max Magnitude0
ClinVar
Risk rs397515817(A;A)
Alt rs397515817(A;A)
Reference rs397515817(G;G)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48756206C>T
CLNSRC ClinVar
CLNACC RCV000035217.2,