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rs267606901

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606901(G;T)
Make rs267606901(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position15726882
GeneMYH11
is asnp
is mentioned by
dbSNPrs267606901
ebirs267606901
HLIrs267606901
Exacrs267606901
Varsomers267606901
Maprs267606901
PheGenIrs267606901
hapmaprs267606901
1000 genomesrs267606901
hgdprs267606901
ensemblrs267606901
gopubmedrs267606901
geneviewrs267606901
scholarrs267606901
googlers267606901
pharmgkbrs267606901
gwascentralrs267606901
openSNPrs267606901
23andMers267606901
23andMe allrs267606901
SNP Nexus

SNPshotrs267606901
SNPdbers267606901
MSV3drs267606901
GWAS Ctlgrs267606901
Max Magnitude0
ClinVar
Risk rs267606901(T;T)
Alt rs267606901(T;T)
Reference rs267606901(G;G)
Significance Pathogenic
Disease Aortic aneurysm
Variation info
Gene MYH11
CLNDBN Aortic aneurysm, familial thoracic 4
Reversed 1
HGVS NC_000016.9:g.15820739C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015195.25,