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rs397515810

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515810(A;A)
Make rs397515810(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48468489
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515810
ebirs397515810
HLIrs397515810
Exacrs397515810
Varsomers397515810
Maprs397515810
PheGenIrs397515810
hapmaprs397515810
1000 genomesrs397515810
hgdprs397515810
ensemblrs397515810
gopubmedrs397515810
geneviewrs397515810
scholarrs397515810
googlers397515810
pharmgkbrs397515810
gwascentralrs397515810
openSNPrs397515810
23andMers397515810
23andMe allrs397515810
SNP Nexus

SNPshotrs397515810
SNPdbers397515810
MSV3drs397515810
GWAS Ctlgrs397515810
Max Magnitude0
ClinVar
Risk rs397515810(A;A)
Alt rs397515810(A;A)
Reference rs397515810(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48760686C>T
CLNSRC ClinVar
CLNACC RCV000035203.2,