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rs794728026

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728026(A;A)
Make rs794728026(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position88941367
GeneACTA2
is asnp
is mentioned by
dbSNPrs794728026
ebirs794728026
HLIrs794728026
Exacrs794728026
Varsomers794728026
Maprs794728026
PheGenIrs794728026
hapmaprs794728026
1000 genomesrs794728026
hgdprs794728026
ensemblrs794728026
gopubmedrs794728026
geneviewrs794728026
scholarrs794728026
googlers794728026
pharmgkbrs794728026
gwascentralrs794728026
openSNPrs794728026
23andMers794728026
23andMe allrs794728026
SNP Nexus

SNPshotrs794728026
SNPdbers794728026
MSV3drs794728026
GWAS Ctlgrs794728026
Max Magnitude0
ClinVar
Risk rs794728026(A;A)
Alt rs794728026(A;A)
Reference Rs794728026(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene ACTA2 STAMBPL1
CLNDBN not specified
Reversed 1
HGVS NC_000010.10:g.90701124C>T
CLNSRC
CLNACC RCV000181022.3,