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

rs1064796483

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position10641151
GeneMYH3
is asnp
is mentioned by
dbSNPrs1064796483
dbSNP (old)rs1064796483
ClinGenrs1064796483
ebirs1064796483
HLIrs1064796483
Exacrs1064796483
Gnomadrs1064796483
Varsomers1064796483
LitVarrs1064796483
Maprs1064796483
PheGenIrs1064796483
Biobankrs1064796483
1000 genomesrs1064796483
hgdprs1064796483
ensemblrs1064796483
gopubmedrs1064796483
geneviewrs1064796483
scholarrs1064796483
googlers1064796483
pharmgkbrs1064796483
gwascentralrs1064796483
openSNPrs1064796483
23andMers1064796483
23andMe allrs1064796483
SNPshotrs1064796483
SNPdbers1064796483
MSV3drs1064796483
GWAS Ctlgrs1064796483
Max Magnitude0
ClinVar
Risk rs1064796483(C;C)
Alt rs1064796483(C;C)
Reference Rs1064796483(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.10544468A>G
CLNSRC
CLNACC RCV000483827.1,