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rs794728019

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728019(A;G)
Make rs794728019(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position88948930
GeneACTA2
is asnp
is mentioned by
dbSNPrs794728019
ebirs794728019
HLIrs794728019
Exacrs794728019
Varsomers794728019
Maprs794728019
PheGenIrs794728019
hapmaprs794728019
1000 genomesrs794728019
hgdprs794728019
ensemblrs794728019
gopubmedrs794728019
geneviewrs794728019
scholarrs794728019
googlers794728019
pharmgkbrs794728019
gwascentralrs794728019
openSNPrs794728019
23andMers794728019
23andMe allrs794728019
SNP Nexus

SNPshotrs794728019
SNPdbers794728019
MSV3drs794728019
GWAS Ctlgrs794728019
Max Magnitude0
ClinVar
Risk rs794728019(G;G)
Alt rs794728019(G;G)
Reference rs794728019(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ACTA2 STAMBPL1
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.90708687T>C
CLNSRC
CLNACC RCV000181012.2,