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rs397515794

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515794(A;A)
Make rs397515794(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48600213
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515794
ebirs397515794
HLIrs397515794
Exacrs397515794
Varsomers397515794
Maprs397515794
PheGenIrs397515794
hapmaprs397515794
1000 genomesrs397515794
hgdprs397515794
ensemblrs397515794
gopubmedrs397515794
geneviewrs397515794
scholarrs397515794
googlers397515794
pharmgkbrs397515794
gwascentralrs397515794
openSNPrs397515794
23andMers397515794
23andMe allrs397515794
SNP Nexus

SNPshotrs397515794
SNPdbers397515794
MSV3drs397515794
GWAS Ctlgrs397515794
Max Magnitude0
ClinVar
Risk rs397515794(A;A)
Alt rs397515794(A;A)
Reference rs397515794(G;G)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48892410C>T
CLNSRC ClinVar
CLNACC RCV000035178.2,