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rs1064793206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position23424993
GeneMYH7
is asnp
is mentioned by
dbSNPrs1064793206
dbSNP (old)rs1064793206
ClinGenrs1064793206
ebirs1064793206
HLIrs1064793206
Exacrs1064793206
Gnomadrs1064793206
Varsomers1064793206
Maprs1064793206
PheGenIrs1064793206
Biobankrs1064793206
1000 genomesrs1064793206
hgdprs1064793206
ensemblrs1064793206
gopubmedrs1064793206
geneviewrs1064793206
scholarrs1064793206
googlers1064793206
pharmgkbrs1064793206
gwascentralrs1064793206
openSNPrs1064793206
23andMers1064793206
23andMe allrs1064793206
SNPshotrs1064793206
SNPdbers1064793206
MSV3drs1064793206
GWAS Ctlgrs1064793206
Max Magnitude0
ClinVar
Risk rs1064793206(T;T)
Alt rs1064793206(T;T)
Reference Rs1064793206(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894202G>A
CLNSRC
CLNACC RCV000484931.1,