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

rs794728023

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728023(A;A)
Make rs794728023(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position88947269
GeneACTA2
is asnp
is mentioned by
dbSNPrs794728023
ebirs794728023
HLIrs794728023
Exacrs794728023
Varsomers794728023
Maprs794728023
PheGenIrs794728023
hapmaprs794728023
1000 genomesrs794728023
hgdprs794728023
ensemblrs794728023
gopubmedrs794728023
geneviewrs794728023
scholarrs794728023
googlers794728023
pharmgkbrs794728023
gwascentralrs794728023
openSNPrs794728023
23andMers794728023
23andMe allrs794728023
SNP Nexus

SNPshotrs794728023
SNPdbers794728023
MSV3drs794728023
GWAS Ctlgrs794728023
Max Magnitude0
ClinVar
Risk rs794728023(A;A)
Alt rs794728023(A;A)
Reference rs794728023(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTA2 STAMBPL1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.90707026C>T
CLNSRC
CLNACC RCV000181017.2,