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rs863223735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223735(A;A)
Make rs863223735(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position67181264
GeneSMAD3
is asnp
is mentioned by
dbSNPrs863223735
dbSNP (classic)rs863223735
ClinGenrs863223735
ebirs863223735
HLIrs863223735
Exacrs863223735
Gnomadrs863223735
Varsomers863223735
LitVarrs863223735
Maprs863223735
PheGenIrs863223735
Biobankrs863223735
1000 genomesrs863223735
hgdprs863223735
ensemblrs863223735
geneviewrs863223735
scholarrs863223735
googlers863223735
pharmgkbrs863223735
gwascentralrs863223735
openSNPrs863223735
23andMers863223735
SNPshotrs863223735
SNPdbers863223735
MSV3drs863223735
GWAS Ctlgrs863223735
Max Magnitude0
ClinVar
Risk rs863223735(A;A)
Alt rs863223735(A;A)
Reference Rs863223735(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.67473602G>A
CLNSRC
CLNACC RCV000196414.2, RCV000476029.1,