Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515325

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515325(A;G)
Make rs397515325(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position88947371
GeneACTA2
is asnp
is mentioned by
dbSNPrs397515325
ebirs397515325
HLIrs397515325
Exacrs397515325
Varsomers397515325
Maprs397515325
PheGenIrs397515325
hapmaprs397515325
1000 genomesrs397515325
hgdprs397515325
ensemblrs397515325
gopubmedrs397515325
geneviewrs397515325
scholarrs397515325
googlers397515325
pharmgkbrs397515325
gwascentralrs397515325
openSNPrs397515325
23andMers397515325
23andMe allrs397515325
SNP Nexus

SNPshotrs397515325
SNPdbers397515325
MSV3drs397515325
GWAS Ctlgrs397515325
Max Magnitude0
ClinVar
Risk rs397515325(G;G)
Alt rs397515325(G;G)
Reference rs397515325(A;A)
Significance Pathogenic
Disease Aortic aneurysm
Variation info
Gene ACTA2 STAMBPL1
CLNDBN Aortic aneurysm, familial thoracic 6
Reversed 1
HGVS NC_000010.10:g.90707128T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000055648.26,