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rs730880879

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880879(A;A)
Make rs730880879(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23427762
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880879
ebirs730880879
HLIrs730880879
Exacrs730880879
Varsomers730880879
Maprs730880879
PheGenIrs730880879
hapmaprs730880879
1000 genomesrs730880879
hgdprs730880879
ensemblrs730880879
gopubmedrs730880879
geneviewrs730880879
scholarrs730880879
googlers730880879
pharmgkbrs730880879
gwascentralrs730880879
openSNPrs730880879
23andMers730880879
23andMe allrs730880879
SNP Nexus

SNPshotrs730880879
SNPdbers730880879
MSV3drs730880879
GWAS Ctlgrs730880879
Max Magnitude0
ClinVar
Risk rs730880879(A;A)
Alt rs730880879(A;A)
Reference rs730880879(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23896971C>T
CLNSRC
CLNACC RCV000158813.1,