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rs1064795023

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position15738685
GeneMYH11
is asnp
is mentioned by
dbSNPrs1064795023
dbSNP (old)rs1064795023
ClinGenrs1064795023
ebirs1064795023
HLIrs1064795023
Exacrs1064795023
Gnomadrs1064795023
Varsomers1064795023
Maprs1064795023
PheGenIrs1064795023
Biobankrs1064795023
1000 genomesrs1064795023
hgdprs1064795023
ensemblrs1064795023
gopubmedrs1064795023
geneviewrs1064795023
scholarrs1064795023
googlers1064795023
pharmgkbrs1064795023
gwascentralrs1064795023
openSNPrs1064795023
23andMers1064795023
23andMe allrs1064795023
SNPshotrs1064795023
SNPdbers1064795023
MSV3drs1064795023
GWAS Ctlgrs1064795023
Max Magnitude0
ClinVar
Risk rs1064795023(T;T)
Alt rs1064795023(T;T)
Reference Rs1064795023(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH11
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.15832542G>A
CLNSRC
CLNACC RCV000485034.1,