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rs878853683

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853683(C;C)
Make rs878853683(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48470639
GeneFBN1
is asnp
is mentioned by
dbSNPrs878853683
ebirs878853683
HLIrs878853683
Exacrs878853683
Varsomers878853683
Maprs878853683
PheGenIrs878853683
hapmaprs878853683
1000 genomesrs878853683
hgdprs878853683
ensemblrs878853683
gopubmedrs878853683
geneviewrs878853683
scholarrs878853683
googlers878853683
pharmgkbrs878853683
gwascentralrs878853683
openSNPrs878853683
23andMers878853683
23andMe allrs878853683
SNP Nexus

SNPshotrs878853683
SNPdbers878853683
MSV3drs878853683
GWAS Ctlgrs878853683
Max Magnitude0
ClinVar
Risk rs878853683(C;C)
Alt rs878853683(C;C)
Reference rs878853683(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48762836C>G
CLNSRC
CLNACC RCV000232283.1,