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rs397515827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515827(A;A)
Make rs397515827(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48446747
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515827
ebirs397515827
HLIrs397515827
Exacrs397515827
Varsomers397515827
Maprs397515827
PheGenIrs397515827
hapmaprs397515827
1000 genomesrs397515827
hgdprs397515827
ensemblrs397515827
gopubmedrs397515827
geneviewrs397515827
scholarrs397515827
googlers397515827
pharmgkbrs397515827
gwascentralrs397515827
openSNPrs397515827
23andMers397515827
23andMe allrs397515827
SNP Nexus

SNPshotrs397515827
SNPdbers397515827
MSV3drs397515827
GWAS Ctlgrs397515827
Max Magnitude0
ClinVar
Risk rs397515827(A;A)
Alt rs397515827(A;A)
Reference rs397515827(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48738944C>T
CLNSRC ClinVar
CLNACC RCV000035233.2,