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rs794728021

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728021(A;A)
Make rs794728021(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position88948815
GeneACTA2
is asnp
is mentioned by
dbSNPrs794728021
ebirs794728021
HLIrs794728021
Exacrs794728021
Varsomers794728021
Maprs794728021
PheGenIrs794728021
hapmaprs794728021
1000 genomesrs794728021
hgdprs794728021
ensemblrs794728021
gopubmedrs794728021
geneviewrs794728021
scholarrs794728021
googlers794728021
pharmgkbrs794728021
gwascentralrs794728021
openSNPrs794728021
23andMers794728021
23andMe allrs794728021
SNP Nexus

SNPshotrs794728021
SNPdbers794728021
MSV3drs794728021
GWAS Ctlgrs794728021
Max Magnitude0
ClinVar
Risk rs794728021(A;A)
Alt rs794728021(A;A)
Reference rs794728021(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTA2 STAMBPL1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.90708572C>T
CLNSRC
CLNACC RCV000181015.2,