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rs869025414

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025414(C;T)
Make rs869025414(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48427630
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025414
ebirs869025414
HLIrs869025414
Exacrs869025414
Varsomers869025414
Maprs869025414
PheGenIrs869025414
hapmaprs869025414
1000 genomesrs869025414
hgdprs869025414
ensemblrs869025414
gopubmedrs869025414
geneviewrs869025414
scholarrs869025414
googlers869025414
pharmgkbrs869025414
gwascentralrs869025414
openSNPrs869025414
23andMers869025414
23andMe allrs869025414
SNP Nexus

SNPshotrs869025414
SNPdbers869025414
MSV3drs869025414
GWAS Ctlgrs869025414
Max Magnitude0
ClinVar
Risk rs869025414(T;T)
Alt rs869025414(T;T)
Reference rs869025414(C;C)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48719827G>A
CLNSRC
CLNACC RCV000208200.1,