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rs397515784

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515784(C;G)
Make rs397515784(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48489921
GeneFBN1
is asnp
is mentioned by
dbSNPrs397515784
ebirs397515784
HLIrs397515784
Exacrs397515784
Varsomers397515784
Maprs397515784
PheGenIrs397515784
hapmaprs397515784
1000 genomesrs397515784
hgdprs397515784
ensemblrs397515784
gopubmedrs397515784
geneviewrs397515784
scholarrs397515784
googlers397515784
pharmgkbrs397515784
gwascentralrs397515784
openSNPrs397515784
23andMers397515784
23andMe allrs397515784
SNP Nexus

SNPshotrs397515784
SNPdbers397515784
MSV3drs397515784
GWAS Ctlgrs397515784
Max Magnitude0
ClinVar
Risk rs397515784(G;G)
Alt rs397515784(G;G)
Reference rs397515784(C;C)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48782118G>C
CLNSRC ClinVar
CLNACC RCV000035159.2,