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rs397515864

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515864(C;G)
Make rs397515864(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48411123
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515864
ebirs397515864
HLIrs397515864
Exacrs397515864
Varsomers397515864
Maprs397515864
PheGenIrs397515864
hapmaprs397515864
1000 genomesrs397515864
hgdprs397515864
ensemblrs397515864
gopubmedrs397515864
geneviewrs397515864
scholarrs397515864
googlers397515864
pharmgkbrs397515864
gwascentralrs397515864
openSNPrs397515864
23andMers397515864
23andMe allrs397515864
SNP Nexus

SNPshotrs397515864
SNPdbers397515864
MSV3drs397515864
GWAS Ctlgrs397515864
Max Magnitude0
ClinVar
Risk rs397515864(G;G)
Alt rs397515864(G;G)
Reference rs397515864(C;C)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48703320G>C
CLNSRC ClinVar
CLNACC RCV000035291.2,