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rs869025413

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025413(C;C)
Make rs869025413(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48430677
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025413
ebirs869025413
HLIrs869025413
Exacrs869025413
Varsomers869025413
Maprs869025413
PheGenIrs869025413
hapmaprs869025413
1000 genomesrs869025413
hgdprs869025413
ensemblrs869025413
gopubmedrs869025413
geneviewrs869025413
scholarrs869025413
googlers869025413
pharmgkbrs869025413
gwascentralrs869025413
openSNPrs869025413
23andMers869025413
23andMe allrs869025413
SNP Nexus

SNPshotrs869025413
SNPdbers869025413
MSV3drs869025413
GWAS Ctlgrs869025413
Max Magnitude0
ClinVar
Risk rs869025413(C;C)
Alt rs869025413(C;C)
Reference rs869025413(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48722874A>G
CLNSRC
CLNACC RCV000208020.1,