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rs878854611

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854611(-;-)
Make rs878854611(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position30691424
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs878854611
ebirs878854611
HLIrs878854611
Exacrs878854611
Varsomers878854611
Maprs878854611
PheGenIrs878854611
hapmaprs878854611
1000 genomesrs878854611
hgdprs878854611
ensemblrs878854611
gopubmedrs878854611
geneviewrs878854611
scholarrs878854611
googlers878854611
pharmgkbrs878854611
gwascentralrs878854611
openSNPrs878854611
23andMers878854611
23andMe allrs878854611
SNP Nexus

SNPshotrs878854611
SNPdbers878854611
MSV3drs878854611
GWAS Ctlgrs878854611
Max Magnitude0
ClinVar
Risk rs878854611(;)
Alt rs878854611(;)
Reference rs878854611(T;T)
Significance Probable-Pathogenic
Disease Thoracic aortic aneurysm and aortic dissection
Variation info
Gene TGFBR2
CLNDBN Thoracic aortic aneurysm and aortic dissection
Reversed 0
HGVS NC_000003.11:g.30732916delT
CLNSRC
CLNACC RCV000227819.1,