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rs730880845

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880845(A;A)
Make rs730880845(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431805
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880845
ebirs730880845
HLIrs730880845
Exacrs730880845
Varsomers730880845
Maprs730880845
PheGenIrs730880845
hapmaprs730880845
1000 genomesrs730880845
hgdprs730880845
ensemblrs730880845
gopubmedrs730880845
geneviewrs730880845
scholarrs730880845
googlers730880845
pharmgkbrs730880845
gwascentralrs730880845
openSNPrs730880845
23andMers730880845
23andMe allrs730880845
SNP Nexus

SNPshotrs730880845
SNPdbers730880845
MSV3drs730880845
GWAS Ctlgrs730880845
Max Magnitude0
ClinVar
Risk rs730880845(A;A)
Alt rs730880845(A;A)
Reference rs730880845(G;G)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23901014C>T
CLNSRC
CLNACC RCV000158745.1,