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rs145105768

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145105768(C;T)
Make rs145105768(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48412724
GeneFBN1
is asnp
is mentioned by
dbSNPrs145105768
ebirs145105768
HLIrs145105768
Exacrs145105768
Varsomers145105768
Maprs145105768
PheGenIrs145105768
hapmaprs145105768
1000 genomesrs145105768
hgdprs145105768
ensemblrs145105768
gopubmedrs145105768
geneviewrs145105768
scholarrs145105768
googlers145105768
pharmgkbrs145105768
gwascentralrs145105768
openSNPrs145105768
23andMers145105768
23andMe allrs145105768
SNP Nexus

SNPshotrs145105768
SNPdbers145105768
MSV3drs145105768
GWAS Ctlgrs145105768
Max Magnitude0
ClinVar
Risk rs145105768(G,T;G,T)
Alt rs145105768(G,T;G,T)
Reference rs145105768(C;C)
Significance Probable-Pathogenic
Disease not specified Thoracic aortic aneurysm and aortic dissection
Variation info
Gene FBN1
CLNDBN not specified Thoracic aortic aneurysm and aortic dissection
Reversed 0
HGVS NC_000015.9:g.48704921C>T
CLNSRC
CLNACC RCV000035284.2, RCV000181626.1,