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rs121434526

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434526(C;T)
Make rs121434526(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position88941794
GeneACTA2
is asnp
is mentioned by
dbSNPrs121434526
ebirs121434526
HLIrs121434526
Exacrs121434526
Varsomers121434526
Maprs121434526
PheGenIrs121434526
hapmaprs121434526
1000 genomesrs121434526
hgdprs121434526
ensemblrs121434526
gopubmedrs121434526
geneviewrs121434526
scholarrs121434526
googlers121434526
pharmgkbrs121434526
gwascentralrs121434526
openSNPrs121434526
23andMers121434526
23andMe allrs121434526
SNP Nexus

SNPshotrs121434526
SNPdbers121434526
MSV3drs121434526
GWAS Ctlgrs121434526
Max Magnitude0
OMIM102620
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434526(T;T)
Alt rs121434526(T;T)
Reference rs121434526(C;C)
Significance Pathogenic
Disease Aortic aneurysm not provided
Variation info
Gene ACTA2 STAMBPL1
CLNDBN Aortic aneurysm, familial thoracic 6 not provided
Reversed 1
HGVS NC_000010.10:g.90701551G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019938.27, RCV000181020.2,