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rs765692335

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765692335(C;C)
Make rs765692335(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48534129
GeneFBN1
is asnp
is mentioned by
dbSNPrs765692335
ebirs765692335
HLIrs765692335
Exacrs765692335
Varsomers765692335
Maprs765692335
PheGenIrs765692335
hapmaprs765692335
1000 genomesrs765692335
hgdprs765692335
ensemblrs765692335
gopubmedrs765692335
geneviewrs765692335
scholarrs765692335
googlers765692335
pharmgkbrs765692335
gwascentralrs765692335
openSNPrs765692335
23andMers765692335
23andMe allrs765692335
SNP Nexus

SNPshotrs765692335
SNPdbers765692335
MSV3drs765692335
GWAS Ctlgrs765692335
Max Magnitude0
ClinVar
Risk rs765692335(C;C)
Alt rs765692335(C;C)
Reference rs765692335(G;G)
Significance Pathogenic
Disease Thoracic aortic aneurysm and aortic dissection
Variation info
Gene FBN1
CLNDBN Thoracic aortic aneurysm and aortic dissection
Reversed 0
HGVS NC_000015.9:g.48826326G>T
CLNSRC
CLNACC RCV000181417.1,