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

rs730880852

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880852(C;G)
Make rs730880852(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431469
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880852
ebirs730880852
HLIrs730880852
Exacrs730880852
Varsomers730880852
Maprs730880852
PheGenIrs730880852
hapmaprs730880852
1000 genomesrs730880852
hgdprs730880852
ensemblrs730880852
gopubmedrs730880852
geneviewrs730880852
scholarrs730880852
googlers730880852
pharmgkbrs730880852
gwascentralrs730880852
openSNPrs730880852
23andMers730880852
23andMe allrs730880852
SNP Nexus

SNPshotrs730880852
SNPdbers730880852
MSV3drs730880852
GWAS Ctlgrs730880852
Max Magnitude0
ClinVar
Risk rs730880852(G;G)
Alt rs730880852(G;G)
Reference rs730880852(C;C)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23900678G>C
CLNSRC
CLNACC RCV000158760.1,