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rs794728031

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728031(C;C)
Make rs794728031(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position88935367
GeneACTA2, ACTA2-AS1
is asnp
is mentioned by
dbSNPrs794728031
ebirs794728031
HLIrs794728031
Exacrs794728031
Varsomers794728031
Maprs794728031
PheGenIrs794728031
hapmaprs794728031
1000 genomesrs794728031
hgdprs794728031
ensemblrs794728031
gopubmedrs794728031
geneviewrs794728031
scholarrs794728031
googlers794728031
pharmgkbrs794728031
gwascentralrs794728031
openSNPrs794728031
23andMers794728031
23andMe allrs794728031
SNP Nexus

SNPshotrs794728031
SNPdbers794728031
MSV3drs794728031
GWAS Ctlgrs794728031
Max Magnitude0
ClinVar
Risk rs794728031(C;C)
Alt rs794728031(C;C)
Reference rs794728031(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTA2 STAMBPL1 ACTA2-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.90695124C>G
CLNSRC
CLNACC RCV000181031.2,