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rs730880844

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880844(A;A)
Make rs730880844(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431837
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880844
ebirs730880844
HLIrs730880844
Exacrs730880844
Varsomers730880844
Maprs730880844
PheGenIrs730880844
hapmaprs730880844
1000 genomesrs730880844
hgdprs730880844
ensemblrs730880844
gopubmedrs730880844
geneviewrs730880844
scholarrs730880844
googlers730880844
pharmgkbrs730880844
gwascentralrs730880844
openSNPrs730880844
23andMers730880844
23andMe allrs730880844
SNP Nexus

SNPshotrs730880844
SNPdbers730880844
MSV3drs730880844
GWAS Ctlgrs730880844
Max Magnitude0
ClinVar
Risk rs730880844(A;A)
Alt rs730880844(A;A)
Reference rs730880844(C;C)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23901046G>T
CLNSRC
CLNACC RCV000158744.1,