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rs397515845

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515845(A;A)
Make rs397515845(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48427677
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515845
ebirs397515845
HLIrs397515845
Exacrs397515845
Varsomers397515845
Maprs397515845
PheGenIrs397515845
hapmaprs397515845
1000 genomesrs397515845
hgdprs397515845
ensemblrs397515845
gopubmedrs397515845
geneviewrs397515845
scholarrs397515845
googlers397515845
pharmgkbrs397515845
gwascentralrs397515845
openSNPrs397515845
23andMers397515845
23andMe allrs397515845
SNP Nexus

SNPshotrs397515845
SNPdbers397515845
MSV3drs397515845
GWAS Ctlgrs397515845
Max Magnitude0
ClinVar
Risk rs397515845(A;A)
Alt rs397515845(A;A)
Reference rs397515845(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48719874C>T
CLNSRC ClinVar
CLNACC RCV000035264.2,