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rs1060500771

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500771(G;T)
Make rs1060500771(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position67166854
GeneSMAD3
is asnp
is mentioned by
dbSNPrs1060500771
dbSNP (old)rs1060500771
ClinGenrs1060500771
ebirs1060500771
HLIrs1060500771
Exacrs1060500771
Gnomadrs1060500771
Varsomers1060500771
Maprs1060500771
PheGenIrs1060500771
Biobankrs1060500771
1000 genomesrs1060500771
hgdprs1060500771
ensemblrs1060500771
gopubmedrs1060500771
geneviewrs1060500771
scholarrs1060500771
googlers1060500771
pharmgkbrs1060500771
gwascentralrs1060500771
openSNPrs1060500771
23andMers1060500771
23andMe allrs1060500771
SNPshotrs1060500771
SNPdbers1060500771
MSV3drs1060500771
GWAS Ctlgrs1060500771
Max Magnitude0
ClinVar
Risk rs1060500771(T;T)
Alt rs1060500771(T;T)
Reference Rs1060500771(G;G)
Significance Probable-Pathogenic
Disease Thoracic aortic aneurysm and aortic dissection
Variation info
Gene SMAD3
CLNDBN Thoracic aortic aneurysm and aortic dissection
Reversed 0
HGVS NC_000015.9:g.67459192G>T
CLNSRC
CLNACC RCV000469786.1,