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rs1064794980

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position10647277
GeneMYH3
is asnp
is mentioned by
dbSNPrs1064794980
dbSNP (old)rs1064794980
ClinGenrs1064794980
ebirs1064794980
HLIrs1064794980
Exacrs1064794980
Gnomadrs1064794980
Varsomers1064794980
Maprs1064794980
PheGenIrs1064794980
Biobankrs1064794980
1000 genomesrs1064794980
hgdprs1064794980
ensemblrs1064794980
gopubmedrs1064794980
geneviewrs1064794980
scholarrs1064794980
googlers1064794980
pharmgkbrs1064794980
gwascentralrs1064794980
openSNPrs1064794980
23andMers1064794980
23andMe allrs1064794980
SNPshotrs1064794980
SNPdbers1064794980
MSV3drs1064794980
GWAS Ctlgrs1064794980
Max Magnitude0
ClinVar
Risk rs1064794980(C;C)
Alt rs1064794980(C;C)
Reference Rs1064794980(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.10550594A>G
CLNSRC
CLNACC RCV000482056.1,