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rs1064793203

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position10640057
GeneMYH3
is asnp
is mentioned by
dbSNPrs1064793203
dbSNP (old)rs1064793203
ClinGenrs1064793203
ebirs1064793203
HLIrs1064793203
Exacrs1064793203
Gnomadrs1064793203
Varsomers1064793203
Maprs1064793203
PheGenIrs1064793203
Biobankrs1064793203
1000 genomesrs1064793203
hgdprs1064793203
ensemblrs1064793203
gopubmedrs1064793203
geneviewrs1064793203
scholarrs1064793203
googlers1064793203
pharmgkbrs1064793203
gwascentralrs1064793203
openSNPrs1064793203
23andMers1064793203
23andMe allrs1064793203
SNPshotrs1064793203
SNPdbers1064793203
MSV3drs1064793203
GWAS Ctlgrs1064793203
Max Magnitude0
ClinVar
Risk rs1064793203(C;C)
Alt rs1064793203(C;C)
Reference Rs1064793203(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.10543374A>G
CLNSRC
CLNACC RCV000479373.1,