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rs730880856

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880856(C;C)
Make rs730880856(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23430954
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880856
ebirs730880856
HLIrs730880856
Exacrs730880856
Varsomers730880856
Maprs730880856
PheGenIrs730880856
hapmaprs730880856
1000 genomesrs730880856
hgdprs730880856
ensemblrs730880856
gopubmedrs730880856
geneviewrs730880856
scholarrs730880856
googlers730880856
pharmgkbrs730880856
gwascentralrs730880856
openSNPrs730880856
23andMers730880856
23andMe allrs730880856
SNP Nexus

SNPshotrs730880856
SNPdbers730880856
MSV3drs730880856
GWAS Ctlgrs730880856
Max Magnitude0
ClinVar
Risk rs730880856(C;C)
Alt rs730880856(C;C)
Reference rs730880856(G;G)
Significance Pathogenic
Disease not provided Primary dilated cardiomyopathy
Variation info
Gene MYH7
CLNDBN not provided Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23900163C>G
CLNSRC
CLNACC RCV000158768.2, RCV000219555.1,