Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728177

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728177(G;T)
Make rs794728177(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48505109
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728177
ebirs794728177
HLIrs794728177
Exacrs794728177
Varsomers794728177
Maprs794728177
PheGenIrs794728177
hapmaprs794728177
1000 genomesrs794728177
hgdprs794728177
ensemblrs794728177
gopubmedrs794728177
geneviewrs794728177
scholarrs794728177
googlers794728177
pharmgkbrs794728177
gwascentralrs794728177
openSNPrs794728177
23andMers794728177
23andMe allrs794728177
SNP Nexus

SNPshotrs794728177
SNPdbers794728177
MSV3drs794728177
GWAS Ctlgrs794728177
Max Magnitude0
ClinVar
Risk rs794728177(T;T)
Alt rs794728177(T;T)
Reference rs794728177(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.48797306C>A
CLNSRC
CLNACC RCV000181445.1,