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rs794728219

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728219(C;T)
Make rs794728219(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48474308
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728219
ebirs794728219
HLIrs794728219
Exacrs794728219
Varsomers794728219
Maprs794728219
PheGenIrs794728219
hapmaprs794728219
1000 genomesrs794728219
hgdprs794728219
ensemblrs794728219
gopubmedrs794728219
geneviewrs794728219
scholarrs794728219
googlers794728219
pharmgkbrs794728219
gwascentralrs794728219
openSNPrs794728219
23andMers794728219
23andMe allrs794728219
SNP Nexus

SNPshotrs794728219
SNPdbers794728219
MSV3drs794728219
GWAS Ctlgrs794728219
Max Magnitude0
ClinVar
Risk rs794728219(T;T)
Alt rs794728219(T;T)
Reference rs794728219(C;C)
Significance Probable-Pathogenic
Disease Thoracic aortic aneurysm and aortic dissection
Variation info
Gene FBN1
CLNDBN Thoracic aortic aneurysm and aortic dissection
Reversed 1
HGVS NC_000015.9:g.48766505G>A
CLNSRC
CLNACC RCV000181511.1,