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rs267606902

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606902(A;A)
Make rs267606902(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position15748092
GeneMYH11
is asnp
is mentioned by
dbSNPrs267606902
ebirs267606902
HLIrs267606902
Exacrs267606902
Varsomers267606902
Maprs267606902
PheGenIrs267606902
hapmaprs267606902
1000 genomesrs267606902
hgdprs267606902
ensemblrs267606902
gopubmedrs267606902
geneviewrs267606902
scholarrs267606902
googlers267606902
pharmgkbrs267606902
gwascentralrs267606902
openSNPrs267606902
23andMers267606902
23andMe allrs267606902
SNP Nexus

SNPshotrs267606902
SNPdbers267606902
MSV3drs267606902
GWAS Ctlgrs267606902
Max Magnitude0
ClinVar
Risk rs267606902(A;A)
Alt rs267606902(A;A)
Reference rs267606902(G;G)
Significance Pathogenic
Disease Aortic aneurysm Thoracic aortic aneurysm and aortic dissection
Variation info
Gene MYH11
CLNDBN Aortic aneurysm, familial thoracic 4 Thoracic aortic aneurysm and aortic dissection
Reversed 1
HGVS NC_000016.9:g.15841949C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015196.25, RCV000157330.1,