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rs201831933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201831933(A;T)
Make rs201831933(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position15726915
GeneMYH11
is asnp
is mentioned by
dbSNPrs201831933
ebirs201831933
HLIrs201831933
Exacrs201831933
Varsomers201831933
Maprs201831933
PheGenIrs201831933
hapmaprs201831933
1000 genomesrs201831933
hgdprs201831933
ensemblrs201831933
gopubmedrs201831933
geneviewrs201831933
scholarrs201831933
googlers201831933
pharmgkbrs201831933
gwascentralrs201831933
openSNPrs201831933
23andMers201831933
23andMe allrs201831933
SNP Nexus

SNPshotrs201831933
SNPdbers201831933
MSV3drs201831933
GWAS Ctlgrs201831933
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs201831933(G,T;G,T)
Alt rs201831933(G,T;G,T)
Reference rs201831933(A;A)
Significance Pathogenic
Disease Aortic aneurysm not provided
Variation info
Gene MYH11
CLNDBN Aortic aneurysm, familial thoracic 4 not provided
Reversed 0
HGVS NC_000016.9:g.15820772A>G
CLNSRC ClinVar GTR
CLNACC RCV000144438.1, RCV000182510.2,