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

rs1060501436

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060501436(C;C)
Make rs1060501436(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position23424815
GeneMYH7
is asnp
is mentioned by
dbSNPrs1060501436
dbSNP (old)rs1060501436
ClinGenrs1060501436
ebirs1060501436
HLIrs1060501436
Exacrs1060501436
Gnomadrs1060501436
Varsomers1060501436
LitVarrs1060501436
Maprs1060501436
PheGenIrs1060501436
Biobankrs1060501436
1000 genomesrs1060501436
hgdprs1060501436
ensemblrs1060501436
gopubmedrs1060501436
geneviewrs1060501436
scholarrs1060501436
googlers1060501436
pharmgkbrs1060501436
gwascentralrs1060501436
openSNPrs1060501436
23andMers1060501436
23andMe allrs1060501436
SNPshotrs1060501436
SNPdbers1060501436
MSV3drs1060501436
GWAS Ctlgrs1060501436
Max Magnitude0
ClinVar
Risk rs1060501436(C;C)
Alt rs1060501436(C;C)
Reference Rs1060501436(T;T)
Significance Probable-Pathogenic
Disease Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23894024A>G
CLNSRC
CLNACC RCV000472927.1,