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rs397515816

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515816(A;A)
Make rs397515816(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48465568
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515816
ebirs397515816
HLIrs397515816
Exacrs397515816
Varsomers397515816
Maprs397515816
PheGenIrs397515816
hapmaprs397515816
1000 genomesrs397515816
hgdprs397515816
ensemblrs397515816
gopubmedrs397515816
geneviewrs397515816
scholarrs397515816
googlers397515816
pharmgkbrs397515816
gwascentralrs397515816
openSNPrs397515816
23andMers397515816
23andMe allrs397515816
SNP Nexus

SNPshotrs397515816
SNPdbers397515816
MSV3drs397515816
GWAS Ctlgrs397515816
Max Magnitude0
ClinVar
Risk rs397515816(A;A)
Alt rs397515816(A;A)
Reference rs397515816(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48757765C>T
CLNSRC ClinVar
CLNACC RCV000035216.2,