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rs794728232

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728232(G;T)
Make rs794728232(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48463982
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728232
ebirs794728232
HLIrs794728232
Exacrs794728232
Varsomers794728232
Maprs794728232
PheGenIrs794728232
hapmaprs794728232
1000 genomesrs794728232
hgdprs794728232
ensemblrs794728232
gopubmedrs794728232
geneviewrs794728232
scholarrs794728232
googlers794728232
pharmgkbrs794728232
gwascentralrs794728232
openSNPrs794728232
23andMers794728232
23andMe allrs794728232
SNP Nexus

SNPshotrs794728232
SNPdbers794728232
MSV3drs794728232
GWAS Ctlgrs794728232
Max Magnitude0
ClinVar
Risk rs794728232(T;T)
Alt rs794728232(T;T)
Reference rs794728232(G;G)
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.48756179C>A
CLNSRC
CLNACC RCV000181536.1,