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rs869025417

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025417(C;C)
Make rs869025417(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48411267
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025417
ebirs869025417
HLIrs869025417
Exacrs869025417
Varsomers869025417
Maprs869025417
PheGenIrs869025417
hapmaprs869025417
1000 genomesrs869025417
hgdprs869025417
ensemblrs869025417
gopubmedrs869025417
geneviewrs869025417
scholarrs869025417
googlers869025417
pharmgkbrs869025417
gwascentralrs869025417
openSNPrs869025417
23andMers869025417
23andMe allrs869025417
SNP Nexus

SNPshotrs869025417
SNPdbers869025417
MSV3drs869025417
GWAS Ctlgrs869025417
Max Magnitude0
ClinVar
Risk rs869025417(C;C)
Alt rs869025417(C;C)
Reference rs869025417(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48703464A>G
CLNSRC
CLNACC RCV000208125.1,