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rs767606368

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs767606368(A;C)
Make rs767606368(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48472673
GeneFBN1
is asnp
is mentioned by
dbSNPrs767606368
ebirs767606368
HLIrs767606368
Exacrs767606368
Varsomers767606368
Maprs767606368
PheGenIrs767606368
hapmaprs767606368
1000 genomesrs767606368
hgdprs767606368
ensemblrs767606368
gopubmedrs767606368
geneviewrs767606368
scholarrs767606368
googlers767606368
pharmgkbrs767606368
gwascentralrs767606368
openSNPrs767606368
23andMers767606368
23andMe allrs767606368
SNP Nexus

SNPshotrs767606368
SNPdbers767606368
MSV3drs767606368
GWAS Ctlgrs767606368
Max Magnitude0
ClinVar
Risk rs767606368(C;C)
Alt rs767606368(C;C)
Reference rs767606368(A;A)
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.48764870A>C
CLNSRC
CLNACC RCV000181513.1,