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rs730880881

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880881(C;T)
Make rs730880881(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23427662
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880881
ebirs730880881
HLIrs730880881
Exacrs730880881
Varsomers730880881
Maprs730880881
PheGenIrs730880881
hapmaprs730880881
1000 genomesrs730880881
hgdprs730880881
ensemblrs730880881
gopubmedrs730880881
geneviewrs730880881
scholarrs730880881
googlers730880881
pharmgkbrs730880881
gwascentralrs730880881
openSNPrs730880881
23andMers730880881
23andMe allrs730880881
SNP Nexus

SNPshotrs730880881
SNPdbers730880881
MSV3drs730880881
GWAS Ctlgrs730880881
Max Magnitude0
ClinVar
Risk rs730880881(T;T)
Alt rs730880881(T;T)
Reference rs730880881(C;C)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23896871G>A
CLNSRC
CLNACC RCV000158818.1,