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rs794728025

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728025(G;T)
Make rs794728025(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position88941793
GeneACTA2
is asnp
is mentioned by
dbSNPrs794728025
ebirs794728025
HLIrs794728025
Exacrs794728025
Varsomers794728025
Maprs794728025
PheGenIrs794728025
hapmaprs794728025
1000 genomesrs794728025
hgdprs794728025
ensemblrs794728025
gopubmedrs794728025
geneviewrs794728025
scholarrs794728025
googlers794728025
pharmgkbrs794728025
gwascentralrs794728025
openSNPrs794728025
23andMers794728025
23andMe allrs794728025
SNP Nexus

SNPshotrs794728025
SNPdbers794728025
MSV3drs794728025
GWAS Ctlgrs794728025
Max Magnitude0
ClinVar
Risk rs794728025(T;T)
Alt rs794728025(T;T)
Reference rs794728025(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTA2 STAMBPL1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.90701550C>A
CLNSRC
CLNACC RCV000181021.2,