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rs794728022

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728022(A;A)
Make rs794728022(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position88947338
GeneACTA2
is asnp
is mentioned by
dbSNPrs794728022
ebirs794728022
HLIrs794728022
Exacrs794728022
Varsomers794728022
Maprs794728022
PheGenIrs794728022
hapmaprs794728022
1000 genomesrs794728022
hgdprs794728022
ensemblrs794728022
gopubmedrs794728022
geneviewrs794728022
scholarrs794728022
googlers794728022
pharmgkbrs794728022
gwascentralrs794728022
openSNPrs794728022
23andMers794728022
23andMe allrs794728022
SNP Nexus

SNPshotrs794728022
SNPdbers794728022
MSV3drs794728022
GWAS Ctlgrs794728022
Max Magnitude0
ClinVar
Risk rs794728022(A;A)
Alt rs794728022(A;A)
Reference rs794728022(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTA2 STAMBPL1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.90707095C>T
CLNSRC
CLNACC RCV000181016.2,