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rs794728275

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728275(A;A)
Make rs794728275(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48421653
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728275
ebirs794728275
HLIrs794728275
Exacrs794728275
Varsomers794728275
Maprs794728275
PheGenIrs794728275
hapmaprs794728275
1000 genomesrs794728275
hgdprs794728275
ensemblrs794728275
gopubmedrs794728275
geneviewrs794728275
scholarrs794728275
googlers794728275
pharmgkbrs794728275
gwascentralrs794728275
openSNPrs794728275
23andMers794728275
23andMe allrs794728275
SNP Nexus

SNPshotrs794728275
SNPdbers794728275
MSV3drs794728275
GWAS Ctlgrs794728275
Max Magnitude0
ClinVar
Risk rs794728275(A;A)
Alt rs794728275(A;A)
Reference rs794728275(G;G)
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.48713850C>T
CLNSRC
CLNACC RCV000181608.1,