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rs371278936

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs371278936(C;C)
Make rs371278936(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48425438
GeneFBN1
is asnp
is mentioned by
dbSNPrs371278936
ebirs371278936
HLIrs371278936
Exacrs371278936
Varsomers371278936
Maprs371278936
PheGenIrs371278936
hapmaprs371278936
1000 genomesrs371278936
hgdprs371278936
ensemblrs371278936
gopubmedrs371278936
geneviewrs371278936
scholarrs371278936
googlers371278936
pharmgkbrs371278936
gwascentralrs371278936
openSNPrs371278936
23andMers371278936
23andMe allrs371278936
SNP Nexus

SNPshotrs371278936
SNPdbers371278936
MSV3drs371278936
GWAS Ctlgrs371278936
Max Magnitude0
ClinVar
Risk rs371278936(C;C)
Alt rs371278936(C;C)
Reference rs371278936(T;T)
Significance Probable-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.48717635T>C
CLNSRC
CLNACC RCV000181601.1,