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rs863223740

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223740(A;A)
Make rs863223740(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67181385
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223740
ebirs863223740
HLIrs863223740
Exacrs863223740
Varsomers863223740
Maprs863223740
PheGenIrs863223740
hapmaprs863223740
1000 genomesrs863223740
hgdprs863223740
ensemblrs863223740
gopubmedrs863223740
geneviewrs863223740
scholarrs863223740
googlers863223740
pharmgkbrs863223740
gwascentralrs863223740
openSNPrs863223740
23andMers863223740
23andMe allrs863223740
SNP Nexus

SNPshotrs863223740
SNPdbers863223740
MSV3drs863223740
GWAS Ctlgrs863223740
Max Magnitude0
ClinVar
Risk rs863223740(A;A)
Alt rs863223740(A;A)
Reference rs863223740(G;G)
Significance Probable-Pathogenic
Disease not specified Thoracic aortic aneurysm and aortic dissection
Variation info
Gene SMAD3
CLNDBN not specified Thoracic aortic aneurysm and aortic dissection
Reversed 0
HGVS NC_000015.9:g.67473723G>A
CLNSRC
CLNACC RCV000197352.2, RCV000222953.1,