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rs878853686

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853686(C;C)
Make rs878853686(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48446811
GeneFBN1
is asnp
is mentioned by
dbSNPrs878853686
ebirs878853686
HLIrs878853686
Exacrs878853686
Varsomers878853686
Maprs878853686
PheGenIrs878853686
hapmaprs878853686
1000 genomesrs878853686
hgdprs878853686
ensemblrs878853686
gopubmedrs878853686
geneviewrs878853686
scholarrs878853686
googlers878853686
pharmgkbrs878853686
gwascentralrs878853686
openSNPrs878853686
23andMers878853686
23andMe allrs878853686
SNP Nexus

SNPshotrs878853686
SNPdbers878853686
MSV3drs878853686
GWAS Ctlgrs878853686
Max Magnitude0
ClinVar
Risk rs878853686(C;C)
Alt rs878853686(C;C)
Reference rs878853686(T;T)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48739008A>G
CLNSRC
CLNACC RCV000227015.1,