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rs878853685

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853685(C;T)
Make rs878853685(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48463926
GeneFBN1
is asnp
is mentioned by
dbSNPrs878853685
ebirs878853685
HLIrs878853685
Exacrs878853685
Varsomers878853685
Maprs878853685
PheGenIrs878853685
hapmaprs878853685
1000 genomesrs878853685
hgdprs878853685
ensemblrs878853685
gopubmedrs878853685
geneviewrs878853685
scholarrs878853685
googlers878853685
pharmgkbrs878853685
gwascentralrs878853685
openSNPrs878853685
23andMers878853685
23andMe allrs878853685
SNP Nexus

SNPshotrs878853685
SNPdbers878853685
MSV3drs878853685
GWAS Ctlgrs878853685
Max Magnitude0
ClinVar
Risk rs878853685(T;T)
Alt rs878853685(T;T)
Reference rs878853685(C;C)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48756123G>A
CLNSRC
CLNACC RCV000232878.1,