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rs1064793205

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome14
Position23425772
GeneMYH7
is asnp
is mentioned by
dbSNPrs1064793205
dbSNP (old)rs1064793205
ClinGenrs1064793205
ebirs1064793205
HLIrs1064793205
Exacrs1064793205
Gnomadrs1064793205
Varsomers1064793205
LitVarrs1064793205
Maprs1064793205
PheGenIrs1064793205
Biobankrs1064793205
1000 genomesrs1064793205
hgdprs1064793205
ensemblrs1064793205
gopubmedrs1064793205
geneviewrs1064793205
scholarrs1064793205
googlers1064793205
pharmgkbrs1064793205
gwascentralrs1064793205
openSNPrs1064793205
23andMers1064793205
23andMe allrs1064793205
SNPshotrs1064793205
SNPdbers1064793205
MSV3drs1064793205
GWAS Ctlgrs1064793205
Max Magnitude0
ClinVar
Risk rs1064793205(T;T)
Alt rs1064793205(T;T)
Reference Rs1064793205(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894981C>A
CLNSRC
CLNACC RCV000480907.1,