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rs730880850

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880850(A;A)
Make rs730880850(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431584
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880850
ebirs730880850
HLIrs730880850
Exacrs730880850
Varsomers730880850
Maprs730880850
PheGenIrs730880850
hapmaprs730880850
1000 genomesrs730880850
hgdprs730880850
ensemblrs730880850
gopubmedrs730880850
geneviewrs730880850
scholarrs730880850
googlers730880850
pharmgkbrs730880850
gwascentralrs730880850
openSNPrs730880850
23andMers730880850
23andMe allrs730880850
SNP Nexus

SNPshotrs730880850
SNPdbers730880850
MSV3drs730880850
GWAS Ctlgrs730880850
Max Magnitude0
ClinVar
Risk rs730880850(A;A)
Alt rs730880850(A;A)
Reference rs730880850(G;G)
Significance Pathogenic
Disease Cardiomyopathy Primary dilated cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy Cardiomyopathy, left ventricular noncompaction Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23900793C>T
CLNSRC
CLNACC RCV000158758.1, RCV000171825.2, RCV000214568.1,