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rs869025404

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025404(C;C)
Make rs869025404(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48505076
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025404
ebirs869025404
HLIrs869025404
Exacrs869025404
Varsomers869025404
Maprs869025404
PheGenIrs869025404
hapmaprs869025404
1000 genomesrs869025404
hgdprs869025404
ensemblrs869025404
gopubmedrs869025404
geneviewrs869025404
scholarrs869025404
googlers869025404
pharmgkbrs869025404
gwascentralrs869025404
openSNPrs869025404
23andMers869025404
23andMe allrs869025404
SNP Nexus

SNPshotrs869025404
SNPdbers869025404
MSV3drs869025404
GWAS Ctlgrs869025404
Max Magnitude0
ClinVar
Risk rs869025404(C;C)
Alt rs869025404(C;C)
Reference rs869025404(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48797273A>G
CLNSRC
CLNACC RCV000208087.1,