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rs886039302

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039302(A;A)
Make rs886039302(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position229432767
GeneACTA1
is asnp
is mentioned by
dbSNPrs886039302
dbSNP (classic)rs886039302
ClinGenrs886039302
ebirs886039302
HLIrs886039302
Exacrs886039302
Gnomadrs886039302
Varsomers886039302
LitVarrs886039302
Maprs886039302
PheGenIrs886039302
Biobankrs886039302
1000 genomesrs886039302
hgdprs886039302
ensemblrs886039302
geneviewrs886039302
scholarrs886039302
googlers886039302
pharmgkbrs886039302
gwascentralrs886039302
openSNPrs886039302
23andMers886039302
23andMe allrs886039302
SNPshotrs886039302
SNPdbers886039302
MSV3drs886039302
GWAS Ctlgrs886039302
Max Magnitude0
ClinVar
Risk rs886039302(A;A)
Alt rs886039302(A;A)
Reference Rs886039302(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTA1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.229568514C>T
CLNSRC
CLNACC RCV000256044.1,