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rs730880895

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880895(A;A)
Make rs730880895(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425373
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880895
ebirs730880895
HLIrs730880895
Exacrs730880895
Varsomers730880895
Maprs730880895
PheGenIrs730880895
hapmaprs730880895
1000 genomesrs730880895
hgdprs730880895
ensemblrs730880895
gopubmedrs730880895
geneviewrs730880895
scholarrs730880895
googlers730880895
pharmgkbrs730880895
gwascentralrs730880895
openSNPrs730880895
23andMers730880895
23andMe allrs730880895
SNP Nexus

SNPshotrs730880895
SNPdbers730880895
MSV3drs730880895
GWAS Ctlgrs730880895
Max Magnitude0
ClinVar
Risk rs730880895(A;A)
Alt rs730880895(A;A)
Reference rs730880895(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23894582C>T
CLNSRC
CLNACC RCV000158839.1,