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rs397514037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514037(G;T)
Make rs397514037(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position15721421
GeneMYH11, NDE1
is asnp
is mentioned by
dbSNPrs397514037
ebirs397514037
HLIrs397514037
Exacrs397514037
Varsomers397514037
Maprs397514037
PheGenIrs397514037
hapmaprs397514037
1000 genomesrs397514037
hgdprs397514037
ensemblrs397514037
gopubmedrs397514037
geneviewrs397514037
scholarrs397514037
googlers397514037
pharmgkbrs397514037
gwascentralrs397514037
openSNPrs397514037
23andMers397514037
23andMe allrs397514037
SNP Nexus

SNPshotrs397514037
SNPdbers397514037
MSV3drs397514037
GWAS Ctlgrs397514037
Max Magnitude0
ClinVar
Risk rs397514037(T;T)
Alt rs397514037(T;T)
Reference rs397514037(G;G)
Significance Pathogenic
Disease Aortic aneurysm
Variation info
Gene NDE1 MYH11
CLNDBN Aortic aneurysm, familial thoracic 4
Reversed 1
HGVS NC_000016.9:g.15815278C>A
CLNSRC ClinVar
CLNACC RCV000015192.25,