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rs869025411

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025411(C;C)
Make rs869025411(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48432911
GeneFBN1
is asnp
is mentioned by
dbSNPrs869025411
ebirs869025411
HLIrs869025411
Exacrs869025411
Varsomers869025411
Maprs869025411
PheGenIrs869025411
hapmaprs869025411
1000 genomesrs869025411
hgdprs869025411
ensemblrs869025411
gopubmedrs869025411
geneviewrs869025411
scholarrs869025411
googlers869025411
pharmgkbrs869025411
gwascentralrs869025411
openSNPrs869025411
23andMers869025411
23andMe allrs869025411
SNP Nexus

SNPshotrs869025411
SNPdbers869025411
MSV3drs869025411
GWAS Ctlgrs869025411
Max Magnitude0
ClinVar
Risk rs869025411(C;C)
Alt rs869025411(C;C)
Reference rs869025411(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48725108A>G
CLNSRC
CLNACC RCV000208180.1,