Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064796729

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome14
Position23425769
GeneMYH7
is asnp
is mentioned by
dbSNPrs1064796729
dbSNP (old)rs1064796729
ClinGenrs1064796729
ebirs1064796729
HLIrs1064796729
Exacrs1064796729
Gnomadrs1064796729
Varsomers1064796729
Maprs1064796729
PheGenIrs1064796729
Biobankrs1064796729
1000 genomesrs1064796729
hgdprs1064796729
ensemblrs1064796729
gopubmedrs1064796729
geneviewrs1064796729
scholarrs1064796729
googlers1064796729
pharmgkbrs1064796729
gwascentralrs1064796729
openSNPrs1064796729
23andMers1064796729
23andMe allrs1064796729
SNPshotrs1064796729
SNPdbers1064796729
MSV3drs1064796729
GWAS Ctlgrs1064796729
Max Magnitude0
ClinVar
Risk rs1064796729(T;T)
Alt rs1064796729(T;T)
Reference Rs1064796729(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894978T>A
CLNSRC
CLNACC RCV000485371.1,