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rs794728677

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728677(-;T)
Make rs794728677(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position15721419
GeneMYH11, NDE1
is asnp
is mentioned by
dbSNPrs794728677
ClinGenrs794728677
ebirs794728677
HLIrs794728677
Exacrs794728677
Varsomers794728677
Maprs794728677
PheGenIrs794728677
hapmaprs794728677
1000 genomesrs794728677
hgdprs794728677
ensemblrs794728677
gopubmedrs794728677
geneviewrs794728677
scholarrs794728677
googlers794728677
pharmgkbrs794728677
gwascentralrs794728677
openSNPrs794728677
23andMers794728677
23andMe allrs794728677
SNP Nexus

SNPshotrs794728677
SNPdbers794728677
MSV3drs794728677
GWAS Ctlgrs794728677
Max Magnitude0
ClinVar
Risk rs794728677(T;T)
Alt rs794728677(T;T)
Reference Rs794728677(;)
Significance Pathogenic
Disease Thoracic aortic aneurysm and aortic dissection
Variation info
Gene NDE1 MYH11
CLNDBN Thoracic aortic aneurysm and aortic dissection
Reversed 1
HGVS NC_000016.9:g.15815277dupA
CLNSRC
CLNACC RCV000182557.1,