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rs886039303

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039303(C;T)
Make rs886039303(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position88941310
GeneACTA2
is asnp
is mentioned by
dbSNPrs886039303
dbSNP (classic)rs886039303
ClinGenrs886039303
ebirs886039303
HLIrs886039303
Exacrs886039303
Gnomadrs886039303
Varsomers886039303
LitVarrs886039303
Maprs886039303
PheGenIrs886039303
Biobankrs886039303
1000 genomesrs886039303
hgdprs886039303
ensemblrs886039303
geneviewrs886039303
scholarrs886039303
googlers886039303
pharmgkbrs886039303
gwascentralrs886039303
openSNPrs886039303
23andMers886039303
SNPshotrs886039303
SNPdbers886039303
MSV3drs886039303
GWAS Ctlgrs886039303
Max Magnitude0
ClinVar
Risk rs886039303(T;T)
Alt rs886039303(T;T)
Reference Rs886039303(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTA2
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.90701067G>A
CLNSRC
CLNACC RCV000255555.1,