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rs397515828

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515828(A;A)
Make rs397515828(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48445453
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515828
ebirs397515828
HLIrs397515828
Exacrs397515828
Varsomers397515828
Maprs397515828
PheGenIrs397515828
hapmaprs397515828
1000 genomesrs397515828
hgdprs397515828
ensemblrs397515828
gopubmedrs397515828
geneviewrs397515828
scholarrs397515828
googlers397515828
pharmgkbrs397515828
gwascentralrs397515828
openSNPrs397515828
23andMers397515828
23andMe allrs397515828
SNP Nexus

SNPshotrs397515828
SNPdbers397515828
MSV3drs397515828
GWAS Ctlgrs397515828
Max Magnitude0
ClinVar
Risk rs397515828(A;A)
Alt rs397515828(A;A)
Reference rs397515828(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48737650C>T
CLNSRC ClinVar
CLNACC RCV000035237.2,