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rs794728276

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728276(C;T)
Make rs794728276(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48421633
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728276
ebirs794728276
HLIrs794728276
Exacrs794728276
Varsomers794728276
Maprs794728276
PheGenIrs794728276
hapmaprs794728276
1000 genomesrs794728276
hgdprs794728276
ensemblrs794728276
gopubmedrs794728276
geneviewrs794728276
scholarrs794728276
googlers794728276
pharmgkbrs794728276
gwascentralrs794728276
openSNPrs794728276
23andMers794728276
23andMe allrs794728276
SNP Nexus

SNPshotrs794728276
SNPdbers794728276
MSV3drs794728276
GWAS Ctlgrs794728276
Max Magnitude0
ClinVar
Risk rs794728276(T;T)
Alt rs794728276(T;T)
Reference rs794728276(C;C)
Significance 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.48713830G>A
CLNSRC
CLNACC RCV000181610.1,