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rs878853689

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853689(A;A)
Make rs878853689(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48537615
GeneFBN1
is asnp
is mentioned by
dbSNPrs878853689
ebirs878853689
HLIrs878853689
Exacrs878853689
Varsomers878853689
Maprs878853689
PheGenIrs878853689
hapmaprs878853689
1000 genomesrs878853689
hgdprs878853689
ensemblrs878853689
gopubmedrs878853689
geneviewrs878853689
scholarrs878853689
googlers878853689
pharmgkbrs878853689
gwascentralrs878853689
openSNPrs878853689
23andMers878853689
23andMe allrs878853689
SNP Nexus

SNPshotrs878853689
SNPdbers878853689
MSV3drs878853689
GWAS Ctlgrs878853689
Max Magnitude0
ClinVar
Risk rs878853689(A;A)
Alt rs878853689(A;A)
Reference rs878853689(T;T)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48829812A>T
CLNSRC
CLNACC RCV000229926.1,