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

rs869025477

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025477(C;T)
Make rs869025477(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23429308
GeneMYH7
is asnp
is mentioned by
dbSNPrs869025477
ebirs869025477
HLIrs869025477
Exacrs869025477
Varsomers869025477
Maprs869025477
PheGenIrs869025477
hapmaprs869025477
1000 genomesrs869025477
hgdprs869025477
ensemblrs869025477
gopubmedrs869025477
geneviewrs869025477
scholarrs869025477
googlers869025477
pharmgkbrs869025477
gwascentralrs869025477
openSNPrs869025477
23andMers869025477
23andMe allrs869025477
SNP Nexus

SNPshotrs869025477
SNPdbers869025477
MSV3drs869025477
GWAS Ctlgrs869025477
Max Magnitude0
ClinVar
Risk rs869025477(T;T)
Alt rs869025477(T;T)
Reference rs869025477(C;C)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23898517G>A
CLNSRC
CLNACC RCV000208016.1,