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rs794728339

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728339(A;G)
Make rs794728339(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48415578
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728339
ebirs794728339
HLIrs794728339
Exacrs794728339
Varsomers794728339
Maprs794728339
PheGenIrs794728339
hapmaprs794728339
1000 genomesrs794728339
hgdprs794728339
ensemblrs794728339
gopubmedrs794728339
geneviewrs794728339
scholarrs794728339
googlers794728339
pharmgkbrs794728339
gwascentralrs794728339
openSNPrs794728339
23andMers794728339
23andMe allrs794728339
SNP Nexus

SNPshotrs794728339
SNPdbers794728339
MSV3drs794728339
GWAS Ctlgrs794728339
Max Magnitude0
ClinVar
Risk rs794728339(G;G)
Alt rs794728339(G;G)
Reference rs794728339(A;A)
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.48707775T>C
CLNSRC
CLNACC RCV000181708.1,