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

rs730880841

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880841(A;A)
Make rs730880841(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432501
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880841
ebirs730880841
HLIrs730880841
Exacrs730880841
Varsomers730880841
Maprs730880841
PheGenIrs730880841
hapmaprs730880841
1000 genomesrs730880841
hgdprs730880841
ensemblrs730880841
gopubmedrs730880841
geneviewrs730880841
scholarrs730880841
googlers730880841
pharmgkbrs730880841
gwascentralrs730880841
openSNPrs730880841
23andMers730880841
23andMe allrs730880841
SNP Nexus

SNPshotrs730880841
SNPdbers730880841
MSV3drs730880841
GWAS Ctlgrs730880841
Max Magnitude0
ClinVar
Risk rs730880841(A;A)
Alt rs730880841(A;A)
Reference rs730880841(G;G)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23901710C>T
CLNSRC
CLNACC RCV000158739.1,