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

rs1064797184

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position23425005
GeneMYH7
is asnp
is mentioned by
dbSNPrs1064797184
dbSNP (old)rs1064797184
ClinGenrs1064797184
ebirs1064797184
HLIrs1064797184
Exacrs1064797184
Gnomadrs1064797184
Varsomers1064797184
Maprs1064797184
PheGenIrs1064797184
Biobankrs1064797184
1000 genomesrs1064797184
hgdprs1064797184
ensemblrs1064797184
gopubmedrs1064797184
geneviewrs1064797184
scholarrs1064797184
googlers1064797184
pharmgkbrs1064797184
gwascentralrs1064797184
openSNPrs1064797184
23andMers1064797184
23andMe allrs1064797184
SNPshotrs1064797184
SNPdbers1064797184
MSV3drs1064797184
GWAS Ctlgrs1064797184
Max Magnitude0
ClinVar
Risk rs1064797184(T;T)
Alt rs1064797184(T;T)
Reference Rs1064797184(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894214G>A
CLNSRC
CLNACC RCV000487997.1,