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rs387906532

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906532(C;C)
Make rs387906532(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position15726936
GeneMYH11
is asnp
is mentioned by
dbSNPrs387906532
ebirs387906532
HLIrs387906532
Exacrs387906532
Varsomers387906532
Maprs387906532
PheGenIrs387906532
hapmaprs387906532
1000 genomesrs387906532
hgdprs387906532
ensemblrs387906532
gopubmedrs387906532
geneviewrs387906532
scholarrs387906532
googlers387906532
pharmgkbrs387906532
gwascentralrs387906532
openSNPrs387906532
23andMers387906532
23andMe allrs387906532
SNP Nexus

SNPshotrs387906532
SNPdbers387906532
MSV3drs387906532
GWAS Ctlgrs387906532
Max Magnitude0
ClinVar
Risk rs387906532(C;C)
Alt rs387906532(C;C)
Reference rs387906532(T;T)
Significance Pathogenic
Disease Aortic aneurysm
Variation info
Gene MYH11
CLNDBN Aortic aneurysm, familial thoracic 4
Reversed 1
HGVS NC_000016.9:g.15820793A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015194.25,