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rs730880877

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880877(A;G)
Make rs730880877(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23427866
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880877
ebirs730880877
HLIrs730880877
Exacrs730880877
Varsomers730880877
Maprs730880877
PheGenIrs730880877
hapmaprs730880877
1000 genomesrs730880877
hgdprs730880877
ensemblrs730880877
gopubmedrs730880877
geneviewrs730880877
scholarrs730880877
googlers730880877
pharmgkbrs730880877
gwascentralrs730880877
openSNPrs730880877
23andMers730880877
23andMe allrs730880877
SNP Nexus

SNPshotrs730880877
SNPdbers730880877
MSV3drs730880877
GWAS Ctlgrs730880877
Max Magnitude0
ClinVar
Risk rs730880877(G;G)
Alt rs730880877(G;G)
Reference rs730880877(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23897075T>C
CLNSRC
CLNACC RCV000158811.1,